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

Agent, Absorbable Hemostatic, Collagen Based

PMA: P800002 · Supplement: S025 · Decision Jun 21, 2019
Classifications
1
FEI Numbers
35
Registration Numbers
35

Basic Information

Device Name
Agent, Absorbable Hemostatic, Collagen Based
Trade Name
Avitene Microfibrillar Collagen Hemostat (MCH) Non-Woven Web and EndoAvitene
PMA Number
P800002
Supplement Number
S025
Device Class
FDA Class 3
Product Code
LMF
Generic Name
Agent, absorbable hemostatic, collagen based
Regulation Number
878.4490
Medical Specialty
General, Plastic Surgery
Advisory Committee
General, Plastic Surgery
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
June 21, 2019
Date Received
May 20, 2019
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Change to in-process manufacturing test methods and in process bioburden monitoring specifications of the Avitene bulk flour component prior to sterilization.

Classifications

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

Product Code Device Name
LMF Agent, Absorbable Hemostatic, Collagen Based