FDA 510(k)

Stryker Orthopaedics Hip Systems Labeling Update

Numéro K : K240418 · 2024-04-12

DemandeurHowmedica Osteonics Corp., Dba Stryker Orthopaedics

Date de décision2024-04-12

Code produitJDI

Comité consultatifOR

DécisionSubstantially Equivalent

Résumé du dispositif

Stryker Orthopaedics Hip Systems Labeling Update is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2024-04-12 under 510(k) number K240418. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Stryker Orthopaedics Hip Systems Labeling Update?

Stryker Orthopaedics Hip Systems Labeling Update is a medical device that received FDA 510(k) clearance on 2024-04-12. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K240418.

When did Stryker Orthopaedics Hip Systems Labeling Update receive FDA 510(k) clearance?

Stryker Orthopaedics Hip Systems Labeling Update received FDA 510(k) clearance on 2024-04-12, under 510(k) number K240418.

Who is the listed applicant for Stryker Orthopaedics Hip Systems Labeling Update?

The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stryker Orthopaedics Hip Systems Labeling Update?

The FDA product code for Stryker Orthopaedics Hip Systems Labeling Update is JDI.

Essais cliniques associés

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Autres dossiers indiquant Howmedica Osteonics Corp., Dba Stryker Orthopaedics en tant que demandeur

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Dispositifs connexes (Code : JDI)

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Source officielle

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