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FDA 510(k)

Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads

K-Number: K192683 · 2020-02-27

ApplicantBiomet UK, Ltd.
Decision Date2020-02-27
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads is a medical device manufactured by Biomet UK, Ltd.. It received FDA 510(k) clearance on 2020-02-27 under approval number K192683. 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 Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads?

Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads is a medical device that received FDA 510(k) clearance on 2020-02-27. It is manufactured by Biomet UK, Ltd.. The 510(k) number is K192683.

When was Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads approved by the FDA?

Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads received FDA 510(k) clearance on 2020-02-27, under approval number K192683.

What company makes Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads?

Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads is manufactured by Biomet UK, Ltd..

What is the FDA product code for Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads?

The FDA product code for Biolox delta Ceramic Heads, Biolox delta Option Ceramic Heads is LZO.

Other Devices by Biomet UK, Ltd.

K200959Biolox® delta Ceramic Heads, Biolox® delta Option Ceramic Heads MR Labeling

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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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