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FDA 510(k)

SMR Finned Short Stems

K-Number: K191963 · 2019-10-10

Decision Date2019-10-10
Product CodeMBF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMR Finned Short Stems is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2019-10-10 under approval number K191963. The device is classified under product code MBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMR Finned Short Stems?

SMR Finned Short Stems is a medical device that received FDA 510(k) clearance on 2019-10-10. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K191963.

When was SMR Finned Short Stems approved by the FDA?

SMR Finned Short Stems received FDA 510(k) clearance on 2019-10-10, under approval number K191963.

What company makes SMR Finned Short Stems?

SMR Finned Short Stems is manufactured by Lima Corporate S.P.A..

What is the FDA product code for SMR Finned Short Stems?

The FDA product code for SMR Finned Short Stems is MBF.

Other Devices by Lima Corporate S.P.A.

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Related Devices (Code: MBF)

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.