SMR 140° Reverse Humeral Body
K-Number: K201905 · 2020-12-17
ApplicantLima Corporate S.P.A.
Decision Date2020-12-17
Product CodeMBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
SMR 140° Reverse Humeral Body is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2020-12-17 under approval number K201905. 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 140° Reverse Humeral Body?
SMR 140° Reverse Humeral Body is a medical device that received FDA 510(k) clearance on 2020-12-17. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K201905.
When was SMR 140° Reverse Humeral Body approved by the FDA?
SMR 140° Reverse Humeral Body received FDA 510(k) clearance on 2020-12-17, under approval number K201905.
What company makes SMR 140° Reverse Humeral Body?
SMR 140° Reverse Humeral Body is manufactured by Lima Corporate S.P.A..
What is the FDA product code for SMR 140° Reverse Humeral Body?
The FDA product code for SMR 140° Reverse Humeral Body is MBF.
Other Devices by Lima Corporate S.P.A.
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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.