FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH

K Number: K851086 · Decision May 21, 1985
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
172
Review Days
64

Basic Information

Device Name
VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH
K Number
K851086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
ETHICON, INC.
Date Received
March 18, 1985
Decision Date
May 21, 1985
Product Code
FTM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FTM Mesh, Surgical

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