FDA 510(k)

Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post

K-Nummer: K232414 · 2023-09-08

AntragstellerTotal Joint Othopedics, Inc.

Entscheidungsdatum2023-09-08

ProduktcodeJWH

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post is the device name listed in this FDA 510(k) record. The listed applicant is Total Joint Othopedics, Inc.. It received FDA 510(k) clearance on 2023-09-08 under 510(k) number K232414. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post?

Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post is a medical device that received FDA 510(k) clearance on 2023-09-08. The listed applicant is Total Joint Othopedics, Inc.. The 510(k) number is K232414.

When did Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post receive FDA 510(k) clearance?

Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post received FDA 510(k) clearance on 2023-09-08, under 510(k) number K232414.

Who is the listed applicant for Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post?

The FDA 510(k) record lists Total Joint Othopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post?

The FDA product code for Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post is JWH.

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Offizielle Quelle

In der FDA-Datenbank anzeigen →

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