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

ExpressBraid Graft Manipulation

K Number: K163651 · Decision Feb 17, 2017
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
93
Review Days
56

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Basic Information

Device Name
ExpressBraid Graft Manipulation
K Number
K163651
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing Corp
Date Received
December 23, 2016
Decision Date
February 17, 2017
Product Code
GAT
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
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

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