TFCC Fast-Fix Kit

FDA 510(k) K132079 · Smith & Nephew, Inc.

Substantially Equivalent

510(k) numberK132079

Submission

Device name
TFCC Fast-Fix Kit
Applicant
Smith & Nephew, Inc.
Andover, MA, US
Received
July 5, 2013
Decision date
December 5, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GAT – Suture, Nonabsorbable, Synthetic, Polyethylene
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5000
Specialty
General, Plastic Surgery
Implant
Yes

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K253024ProZip Knotless ImplantGAT · Special Riverpoint Medical10/16/2025SE
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K252201HS FiberGAT · Special Riverpoint Medical08/13/2025SE
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K243608TRIGEN Stable Lock Nut & WasherJDS · Traditional 06/12/2025SE
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Questions and answers

When was TFCC Fast-Fix Kit cleared by the FDA?

TFCC Fast-Fix Kit (K132079) received a 510(k) decision of Substantially Equivalent on December 5, 2013, 153 days after the submission was received.

What is the product code of K132079?

The FDA product code is GAT – Suture, Nonabsorbable, Synthetic, Polyethylene, a Class II (moderate risk) device regulated under 21 CFR 878.5000.