FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Dressing, Wound And Burn, Interactive

PMA: P900033 · Supplement: S105 · Decision Feb 23, 2023
Classifications
1
FEI Numbers
6
Registration Numbers
6

Basic Information

Device Name
Dressing, Wound And Burn, Interactive
Trade Name
Integra Dermal Regeneration Template - Terminally Sterilized, Integra Meshed Dermal Regeneration Template - Terminally S
PMA Number
P900033
Supplement Number
S105
Device Class
FDA Class 3
Product Code
MGR
Generic Name
Dressing, wound and burn, interactive
Medical Specialty
Unknown
Advisory Committee
General, Plastic Surgery
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
February 23, 2023
Date Received
January 27, 2023
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Replacement of the current stainless-steel AT basket/paddle with a modular polyethylene/stainless steel AT basket to improve ergonomics and reduce wear particles as a result of paddle motion at the Integra LifeSciences Collagen Manufacturing Center located at 105 Morgan Lane, Plainsboro, NJ 08536.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MGR Dressing, Wound And Burn, Interactive