FDA 510(k)

Catalyst CSR Shoulder System

Numéro K : K152825 · 2016-05-11

Date de décision2016-05-11

Code produitKWT

Comité consultatifOR

DécisionSubstantially Equivalent

Résumé du dispositif

Catalyst CSR Shoulder System is the device name listed in this FDA 510(k) record. The listed applicant is Catalyst Orthoscience, LLC. It received FDA 510(k) clearance on 2016-05-11 under 510(k) number K152825. The device is classified under product code KWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Catalyst CSR Shoulder System?

Catalyst CSR Shoulder System is a medical device that received FDA 510(k) clearance on 2016-05-11. The listed applicant is Catalyst Orthoscience, LLC. The 510(k) number is K152825.

When did Catalyst CSR Shoulder System receive FDA 510(k) clearance?

Catalyst CSR Shoulder System received FDA 510(k) clearance on 2016-05-11, under 510(k) number K152825.

Who is the listed applicant for Catalyst CSR Shoulder System?

The FDA 510(k) record lists Catalyst Orthoscience, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Catalyst CSR Shoulder System?

The FDA product code for Catalyst CSR Shoulder System is KWT.

Essais cliniques associés

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Dispositifs connexes (Code : KWT)

K262173N22 Offset Humeral HeadShoulder Innovations, Inc.K250713Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder ImplantsExactech, Inc.K251686Tornier Humeral Reconstruction System Max (Tornier HRS Max)Tornier, Inc.K241944AGILON® XO Shoulder Replacement SystemImplantcast GmbH K241817InSet Total Shoulder SystemShoulder Innovations, Inc.K231657AGILON® XO Shoulder Replacement SystemImplantcast GmbH

Source officielle

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