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FDA 510(k)

DEPUY CAS KNEE INSTRUMENTATION

K-Number: K043223 · 2005-03-04

ApplicantDePuy Orthopaedics, Inc.
Decision Date2005-03-04
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DEPUY CAS KNEE INSTRUMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2005-03-04 under 510(k) number K043223. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY CAS KNEE INSTRUMENTATION?

DEPUY CAS KNEE INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 2005-03-04. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K043223.

When did DEPUY CAS KNEE INSTRUMENTATION receive FDA 510(k) clearance?

DEPUY CAS KNEE INSTRUMENTATION received FDA 510(k) clearance on 2005-03-04, under 510(k) number K043223.

Who is the listed applicant for DEPUY CAS KNEE INSTRUMENTATION?

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

What is the FDA product code for DEPUY CAS KNEE INSTRUMENTATION?

The FDA product code for DEPUY CAS KNEE INSTRUMENTATION is HAW.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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