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FDA 510(k)

StageOne Knee Cement Spacer Molds

K-Number: K213287 · 2022-09-02

ApplicantBiomet, Inc.
Decision Date2022-09-02
Product CodeMBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

StageOne Knee Cement Spacer Molds is a medical device manufactured by Biomet, Inc.. It received FDA 510(k) clearance on 2022-09-02 under approval number K213287. The device is classified under product code MBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the StageOne Knee Cement Spacer Molds?

StageOne Knee Cement Spacer Molds is a medical device that received FDA 510(k) clearance on 2022-09-02. It is manufactured by Biomet, Inc.. The 510(k) number is K213287.

When was StageOne Knee Cement Spacer Molds approved by the FDA?

StageOne Knee Cement Spacer Molds received FDA 510(k) clearance on 2022-09-02, under approval number K213287.

What company makes StageOne Knee Cement Spacer Molds?

StageOne Knee Cement Spacer Molds is manufactured by Biomet, Inc..

What is the FDA product code for StageOne Knee Cement Spacer Molds?

The FDA product code for StageOne Knee Cement Spacer Molds is MBB.

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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.