5-3/4" SIDE CUTTING NEEDLEHOLDER T/C

POUCH RACK LOOP STYLE 5 SLOT 1.625" SPACING 8.7 x 4 x 4

POUCH RACK LOOP STYLE 21 SLOT 0.75" SPACING 16.3 X 4 X 4

POUCH RACK LOOP STYLE 10 SLOT 1.625" SPACING 16.8 x 4 x 4

POUCH RACK LOOP STYLE 4 SLOT 5" SPACING 20.5 X 6 X 6

POUCH RACK LOOP STYLE 8 SLOT 2.5" SPACING 20.5 X 6 X 6

POUCH RACK PEG STYLE 4 SLOT 4" SPACING 16.5 X 7.25 X 4

POUCH RACK PEG STYLE 4" SPACING 20.5 x 7.25 x 4 /5 SLOT

10" L x 2.75" W BALL & SOCKET INSTRUMENT STRINGER

Instrument: Drill and Screw Guide Holding Screw. The Radian MIS Bunion System is intended for fixation of osteotomies and corrective procedures of the hallux and associated disorders such as hallux valgus.

EARP DISC RAKEThe 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.

EARP DISC RAKE ANGLED. 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.

EARP, TRIAL 18X35X14 12° 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.

EARP, TRIAL 22X35X10 6° 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.

EARP, TRIAL 22X35X12 6° 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.

EARP, TRIAL 22X35X14 6° 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.

EARP, TRIAL 22X35X12 12° 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.

EARP, TRIAL 22X35X14 12° 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.

SUCTION TUBE POOLE STRAIGHT 5.5MMØ 17 FR.8"

SUCTION TUBE YANKAUER 3MMØ COMPLETE 10.5"

SCALPEL HANDLE ANGLED #3L

PROBE BUTTONED WITH EYE 2MMØ 5.75"

DIRECTOR GROOVED 5.75"

PROBE/DIRECTORLOCKHART-MUMMERY FISTULA CURVED 6.5"

BURR SPHERICAL FOR HUDSON BONE HAND DRILL 22MM (34241-00)

HANDLE FOR WIRE SAW GIGLI

SUCTION TUBE FRAZIER-FERGUSSON 30° CHARR. 9 7.5"

ANTRUM CANNULA EICKEN (KILLIAN) 3MM SHORT CURVE STAINLESS STEEL 5.5"

SEPARATOR SMITH RAMUS 9.25"

SPLIT SEPARATORS SMITH SAGITTAL LEFT 9MM 7.25"

RIB SHEAR BETHUNE 13.5"

RIB CONTRACTOR BAILEY-GIBBON LONG CLAWS 6.25"

CIRCUMCISION INSTRUMENT MOGEN 2.5MM 3"

LIGATOR HAEMORRHOIDAL SUCTION COMPLETE WITH 2 ASPIRATION TIPS 69458-11 & 69458-16 AND CHARGING CONE 69458-10

UTERINE DILATOR HEGAR DOUBLE ENDED 3/4MMØ

EXCAVATOR WITH HOLE DOUBLE ENDED 1.5MM / 2MM 5.75"

ROUND BOWL STAINLESS STEEL .35 LITERS 4.5" X 2"