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

COLLAGEN TENDON WRAP

K Number: K080452 · Decision May 15, 2008
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
47
Review Days
86

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Basic Information

Device Name
COLLAGEN TENDON WRAP
K Number
K080452
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
Collagen Matrix, Inc.
Date Received
February 19, 2008
Decision Date
May 15, 2008
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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