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

CAPSEW PLICATION SYSTEM

K Number: K071796 · Decision Oct 19, 2007
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
22
Review Days
109

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Basic Information

Device Name
CAPSEW PLICATION SYSTEM
K Number
K071796
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
Cayenne Medical, Inc.
Date Received
July 2, 2007
Decision Date
October 19, 2007
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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Other Clearances by Cayenne Medical, Inc.

K Number Device Name
K180274 Ventix Link Knotless Anchor with Inserter
K172186 BioWick X Implant with Driver
K161033 AFX™ Femoral Implant With Inserter
K151068 SureLock W Suture Anchor
K143473 Short SureLock All-Suture Anchor, 1.4mm with (1) size 0 UHMWPE suture with needles, Short SureLock All-Suture Anchor, 1.4mm with (1) size 2-0 UHMWPE suture with needles
K143392 Quattro Bolt Tenodesis Screw
K132867 SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 1.4MM, SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 2.2MM
K131325 QUATTRO GL SUTURE ANCHOR
K122314 QUATRO LINK KNOTLESS ANCHOR WITH INSERTER, 2.9MM-PEEK ONLY
K122463 APERFIX AM FEMORAL IMPLANT WITH INSERTER, 9X24 APERFIX AM FEMORAL IMPLANT WITH INSERTER, 10X24 APERFIX FEMORAL IMPLANT W
Search all 22 clearances from Cayenne Medical, Inc. →