Bioinductive Implant with Arthroscopic Delivery System - Large - 4566
Device Description
A bioabsorbable, implantable material (e.g., flat sheet) made from animal-derived collagen intended for extra-gynaecological, non-dental tissue repair/reinforcement application(s) [e.g., pericardial reinforcement, plastic surgery, abdominal hernia repair]; some types may also be intended for use as a short-term scaffold for tissue regeneration. It is constructed of collagen, which might be cross-linked (e.g., with glutaraldehyde); it does not include antimicrobial agents/materials. Disposable devices associated with implantation may be supplied with the mesh.
Environmental Conditions
- 86.00
- 59.00
- 30.00
- 15.00
Device Sizes
No Data Available
Device Sterilization
Device Sterile: True
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: ORQ
Device Name: Mesh, Surgical, Deployer
Device Class: 2
Physical State: manual laparoscopic surgical instrument ;operation handle and deployment section.
Definition: Intended to be used to facilitate the delivery of soft tissue prosthetics during the laparoscopic repair of soft tissue defects (e.G. Hernia repair).
Submission Type ID: 1
Review Panel: SU
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: intended to facilitate hernia mesh delivery and placement during laparoscopic ventral hernia repair.
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: abdominal cavity
Regulation Number: 878.3300
Third Party Flag: N
Medical Specialty: SU
Code: OWY
Device Name: Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Device Class: 2
Physical State: A collagen mesh; either square, rectangular, round or of various other shapes.
Definition: For reinforcement of soft tissue where weakness exists in tendon repair.
Submission Type ID: 1
Review Panel: OR
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: A collagen mesh that reinforces soft tissue.
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: Y
Target Area: Tendon
Regulation Number: 878.3300
Third Party Flag: N
Medical Specialty: SU
Device IdentifiersDevice Id: 00885556735664
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A
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