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FDA 510(k)

CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET

K-Number: K033519 · 2003-12-05

ApplicantBiomet, Inc.
Decision Date2003-12-05
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2003-12-05 under 510(k) number K033519. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET?

CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET is a medical device that received FDA 510(k) clearance on 2003-12-05. The listed applicant is Biomet, Inc.. The 510(k) number is K033519.

When did CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET receive FDA 510(k) clearance?

CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET received FDA 510(k) clearance on 2003-12-05, under 510(k) number K033519.

Who is the listed applicant for CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET?

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

What is the FDA product code for CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET?

The FDA product code for CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET is HRS.

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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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