C2 femoral stem
K-Number: K170473 · 2017-11-08
ApplicantLima Corporate S.P.A.
Decision Date2017-11-08
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
C2 femoral stem is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2017-11-08 under approval number K170473. 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 C2 femoral stem?
C2 femoral stem is a medical device that received FDA 510(k) clearance on 2017-11-08. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K170473.
When was C2 femoral stem approved by the FDA?
C2 femoral stem received FDA 510(k) clearance on 2017-11-08, under approval number K170473.
What company makes C2 femoral stem?
C2 femoral stem is manufactured by Lima Corporate S.P.A..
What is the FDA product code for C2 femoral stem?
The FDA product code for C2 femoral stem is LZO.
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.