Klockner Abutments
K-Number: K230103 · 2023-04-24
ApplicantSOADCO, S.L.
Decision Date2023-04-24
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Klockner Abutments is a medical device manufactured by SOADCO, S.L.. It received FDA 510(k) clearance on 2023-04-24 under approval number K230103. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Klockner Abutments?
Klockner Abutments is a medical device that received FDA 510(k) clearance on 2023-04-24. It is manufactured by SOADCO, S.L.. The 510(k) number is K230103.
When was Klockner Abutments approved by the FDA?
Klockner Abutments received FDA 510(k) clearance on 2023-04-24, under approval number K230103.
What company makes Klockner Abutments?
Klockner Abutments is manufactured by SOADCO, S.L..
What is the FDA product code for Klockner Abutments?
The FDA product code for Klockner Abutments is NHA.
Other Devices by SOADCO, S.L.
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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.