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 a medical device manufactured by Biomet Orthopedics. It received FDA 510(k) clearance on 2020-12-08 under approval 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. It is manufactured by Biomet Orthopedics. The 510(k) number is K200196.

When was Taperloc® Complete Hip Stems approved by the FDA?

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

What company makes Taperloc® Complete Hip Stems?

Taperloc® Complete Hip Stems is manufactured by Biomet Orthopedics.

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

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

Other Devices by Biomet Orthopedics

K223631Comprehensive Segmental Revision System(SRS) K243761A.L.P.S. Small Fragment Plating System K252404Comprehensive Reverse Shoulder - HA Glenosphere Baseplates

Related Devices (Code: LZO)

K160895Initia Total Hip System & BIOCERAM AZUL(R) HEADKyocera Medical Corporation K161830Zimmer M/L Taper Hip ProsthesisZimmer, Inc. K161192Wagner SL Revision Stem Lateral, Wagner Cone Prosthesis® SystemZimmer GmbH K152893Corin Optimized Positioning System (OPS)Corin USA K160289MasterLoc StemMedacta International K152903REVIVAL(TM) Modular Revision Hip StemCorin USA

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.