LimaCorporate Kirschner Wire
K-Number: K203475 · 2021-02-05
ApplicantLima Corporate S.P.A.
Decision Date2021-02-05
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
LimaCorporate Kirschner Wire is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2021-02-05 under approval number K203475. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LimaCorporate Kirschner Wire?
LimaCorporate Kirschner Wire is a medical device that received FDA 510(k) clearance on 2021-02-05. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K203475.
When was LimaCorporate Kirschner Wire approved by the FDA?
LimaCorporate Kirschner Wire received FDA 510(k) clearance on 2021-02-05, under approval number K203475.
What company makes LimaCorporate Kirschner Wire?
LimaCorporate Kirschner Wire is manufactured by Lima Corporate S.P.A..
What is the FDA product code for LimaCorporate Kirschner Wire?
The FDA product code for LimaCorporate Kirschner Wire is HTY.
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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.