3M™ Steri-Drape™ Pouch with Ioban™ 2 Incise Film 6657

DISPS KIT,TRANS-TIB ACL W/ SAWBLD

9MM TENDON STRIPPER BLADE

MENISCAL CINCH™ II

EXCALIBUR, CURVED, HL 4.2MM X 19CM

2-0 FIBERWIRE MENISCUS REPAIR NEEDLES

DISSECTOR, CURVED 3.5MM X 13CM

BONE CUTTER,3.8MM X 13CM

EXCALIBUR, CURVED 4.0MM X 13CM

DOUBLECUT, 4.0MM X 13CM

EXCALIBUR, 5.5MM 13CM

BURR, OVAL, 12 FLUTE 5.5MM X 13CM

Sabre, 2.0mm x 7cm

Bard 3DMax Mesh Left Extra Large

Bard 3DMax Mesh Right Medium

Ventralex ST Hernia Patch

3.5MM STERLING, FULL RADIUS RESECTOR MICROBLADE

THERMOGARD DUAL DISPERSIVE ELECTRODE, CONTACT QUALITY MONITOR

4.2MM GREAT WHITE, SMALL HUB BLADE

4.2MM MERLIN GATOR, SMALL HUB

Fixation Device;15 Violet Absorbable Tacks

Composite Ventral Patch;Polyester & Polyglycolic-Lactic Acid Patch with Absorbable Collagen Film

SorbaFix Absorbable Fixation System 15 Absorbable Fasteners

Ventralight ST Mesh

Ventralight ST Mesh

Ventralight ST Mesh with Echo PS Positioning System

VAPR COOLPULSE 90 Electrode with Hand Controls 90 DEGREES Suction with Integrated Handpiece

Black Monofilament Nylon, Nonabsorbable Surgical Suture

Undyed Braided (Polyglactin 910), Synthetic Absorbable Surgical Suture

Blue Monofilament (Polypropylene), Nonabsorbable Surgical Suture

LIGACLIP MCA Multiple Clip Appliers, 20 Small Clips

ENSEAL X1 Tissue Sealer, Curved Jaw, 37 cm Shaft Length

ENSEAL X1 STRAIGHT 37CM SHAFT

The ECHELON FLEX Powered Plus Articulating Endoscopic Linear Cutters are sterile, single patient use instruments that simultaneouslycut and staple tissue. There are six staggered rows of staples, three on either side of the cut line. The ECHELON FLEX 45 Powered Plusinstruments have a staple line that is approximately 45 mm long and a cut line that is approximately 42 mm long. The shaft can rotate freelyin both directions and an articulation mechanism enables the distal portion of the shaft to pivot to facilitate lateral access to the operativesite.The instruments are packaged with a primary lithium battery pack that must be installed prior to use. There are specific requirements fordisposing of the battery pack. Refer to the Battery Pack Disposal section.The instruments are packaged without a reload and must be loaded prior to use. A staple retaining cap on the reload protects the staple legpoints during shipping and transportation. The instruments’ lock-out feature is designed to prevent a used or improperly installed reloadfrom being refired or an instrument from being fired without a reload.

Integra® Jarit® Crile Forceps, 5-3/4", Straight, Satin Finish

Integra® Jarit® Foerster Sponge Holding Forceps, 9-3/4", Straight, Serrated Jaws, Satin Finish

Integra® Jarit® Allis Forceps, 7-1/2", Tissue, 5x6 Teeth

Integra® Jarit® Cushing Vein Retractor, 9", 11.4mm Wide, 12.45mm Deep

CODMAN® ISOCOOL® AHT® Bipolar Forceps Tips 8 1/2" (22cm) Total Length 0.5mm Tip Diameter 3 1/2" (8.9cm) Working Length

CODMAN® ISOCOOL® AHT® Bipolar Forceps Tips 10 1/2" (26.7cm) Total Length 0.5mm Tip Diameter 5 1/2" (14cm) Working Length

Polypropylene partially absorbable oval blue / undyed Mesh Device

Sponge: Specialty Tonsil XR Med 100/cs

FAST-FIX 360 STRAIGHT MENISCAL REPAIR SYSTEM

FAST-FIX 360 CURVED MENISCAL REPAIR SYSTEM

Composite Mesh,Monofilament Polyester with Absorbable Collagen Film and Marking

Self-Gripping Polyester Mesh,Left Anatomical, Polyester with Polylactic Acid Grips

Self-Gripping Polyester Mesh,Right Anatomical, Polyester with Polylactic Acid Grips

Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s

Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s