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

CROSSFIX II MEMISCAL REPAIR DEVICE

K Number: K121413 · Decision Jun 4, 2012
Classifications
1
FEI Numbers
233
Registration Numbers
233
Same Product Code
166
Applicant Total
17
Review Days
24

Basic Information

Device Name
CROSSFIX II MEMISCAL REPAIR DEVICE
K Number
K121413
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CAYENNE MEDICAL, INC.
Date Received
May 11, 2012
Decision Date
June 4, 2012
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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