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

SEPRAMESH, MODEL 5959-1214

K Number: K063739 · Decision Jan 17, 2007
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
6
Review Days
30

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Basic Information

Device Name
SEPRAMESH, MODEL 5959-1214
K Number
K063739
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 Corporation
Date Received
December 18, 2006
Decision Date
January 17, 2007
Product Code
FTL
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
FTL Mesh, Surgical, Polymeric

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K053066 SEPRAMESH IP BIORESORBABLE COATING/PERMANENT MESH
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