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FDA 510(k)

TAPERLOC COMPLETE, SIZE 5 AND 6

K-Number: K103755 · 2011-01-21

Decision Date2011-01-21
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TAPERLOC COMPLETE, SIZE 5 AND 6 is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2011-01-21 under 510(k) number K103755. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAPERLOC COMPLETE, SIZE 5 AND 6?

TAPERLOC COMPLETE, SIZE 5 AND 6 is a medical device that received FDA 510(k) clearance on 2011-01-21. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K103755.

When did TAPERLOC COMPLETE, SIZE 5 AND 6 receive FDA 510(k) clearance?

TAPERLOC COMPLETE, SIZE 5 AND 6 received FDA 510(k) clearance on 2011-01-21, under 510(k) number K103755.

Who is the listed applicant for TAPERLOC COMPLETE, SIZE 5 AND 6?

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

What is the FDA product code for TAPERLOC COMPLETE, SIZE 5 AND 6?

The FDA product code for TAPERLOC COMPLETE, SIZE 5 AND 6 is KWA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Biomet Manufacturing Corp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KWA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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