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FDA 510(k)

Taperloc® Complete Hip Stems

K-Number: K200196 · 2020-12-08

Decision Date2020-12-08
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Taperloc® Complete Hip Stems is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics. It received FDA 510(k) clearance on 2020-12-08 under 510(k) number K200196. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Taperloc® Complete Hip Stems?

Taperloc® Complete Hip Stems is a medical device that received FDA 510(k) clearance on 2020-12-08. The listed applicant is Biomet Orthopedics. The 510(k) number is K200196.

When did Taperloc® Complete Hip Stems receive FDA 510(k) clearance?

Taperloc® Complete Hip Stems received FDA 510(k) clearance on 2020-12-08, under 510(k) number K200196.

Who is the listed applicant for Taperloc® Complete Hip Stems?

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

What is the FDA product code for Taperloc® Complete Hip Stems?

The FDA product code for Taperloc® Complete Hip Stems is LZO.

Other records listing Biomet Orthopedics 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.

Related Devices (Code: LZO)

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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