EARP DISC SPACER 8MM The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP DISC SPACER 10MM The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP DISC SPACER 12MM The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP DISC SPACER 14MM The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP DISC SPACER INSERTER. The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP FINAL INSERTER. The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP INITIAL INSERTER. The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

RETRACTABLE OSTEOTOME. The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDDpatients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

EARP Retractor, EARP BLADE 100The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 110. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 120. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 130. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 140. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 150. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 60. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 70. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 80. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP BLADE 90. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP CRADLE ASSEMBLY.The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP Retractor, EARP RETRACTOR CONNECTOR.The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.

EARP, 14X25X08 0° The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDD patients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.

Retropsoas Electrode, NERVE CUFF ELECTRODE, 4MM The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Retropsoas Electrode, NERVE CUFF ELECTRODE, 6MM The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Retropsoas Electrode, NERVE CUFF ELECTRODE, 8MM The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Retropsoas Electrode, NERVE CUFF ELECTRODE, 10MM The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Retropsoas Electrode, NERVE CUFF APPLICATOR. The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Retropsoas Electrode, NERVE CUFF TRIAL SIZER, 4/6MM. The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

Retropsoas Electrode, NERVE CUFF TRIAL SIZER, 8/10MM. The EARP Nerve Cuff Electrode is used to perform localized stimulation of neural tissue and to locate, identify, and monitor spinal nerve roots during surgery.

8mm (2° Sagittal 10° Transverse) Lapidus Wedge . The Trigon HA Stand-Alone Wedge Fixagtion System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

8mm (4° Sagittal 4° Transverse) Lapidus Wedge . The Trigon HA Stand-Alone Wedge Fixagtion System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

8mm (4° Sagittal 6° Transverse) Lapidus Wedge . The Trigon HA Stand-Alone Wedge Fixagtion System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

8mm (4° Sagittal 8° Transverse) Lapidus Wedge . The Trigon HA Stand-Alone Wedge Fixagtion System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

8mm (4° Sagittal 10° Transverse) Lapidus Wedge . The Trigon HA Stand-Alone Wedge Fixagtion System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Implant 6mm PEEK Subtalar Wedge. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Implant 8mm PEEK Subtalar Wedge. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Implant 10mm PEEK Subtalar Wedge. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Implant 12mm PEEK Subtalar Wedge. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Implant 14mm PEEK Subtalar Wedge. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Implant 16mm PEEK Subtalar Wedge. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Trigon Subtalar Graft Packing Block. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Trigon Subtalar Wedge Case Assembly. The Trigon HA Stand-Alone Wedge Fixation System is a family of wedges used for angular correction of small bones of the foot. The HA PEEK wedges w/ tantalum markers are provided in multiple footprint and thickness designs, and the titanium bone screws are available in multiple lengths to accommodate variations in patient anatomy.

Instrument: Subtalar Calc Targeting Jig Angle. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar Calc Targeting Jig Straight. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar Wedge Inserter. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar 6mm Trial. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar 8mm Trial. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar 10mm Trial. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar 12mm Trial. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar 14mm Trial. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.

Instrument: Subtalar 16mm Trial. The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as:• Cotton ( opening wedge) Osteotomies of the Medial Cuneiform• Evans Lengthening Osteotomies• Subtalar Fusion• First Metatarsal-Cuneiform Lengthening Arthrodesis• Calcaneocuboid ArthrodesisThe Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine.