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

SEPRAMESH IP BIORESORBABLE BARRIER - PERMANENT MESH

K Number: K040868 · Decision Jun 4, 2004
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
27
Review Days
63

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Basic Information

Device Name
SEPRAMESH IP BIORESORBABLE BARRIER - PERMANENT MESH
K Number
K040868
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genzyme Corp.
Date Received
April 2, 2004
Decision Date
June 4, 2004
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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