Klockner Vega TiBase for CEREC
K-Number: K170022 · 2017-11-16
ApplicantSOADCO, S.L.
Decision Date2017-11-16
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Klockner Vega TiBase for CEREC is a medical device manufactured by SOADCO, S.L.. It received FDA 510(k) clearance on 2017-11-16 under approval number K170022. 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 Vega TiBase for CEREC?
Klockner Vega TiBase for CEREC is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by SOADCO, S.L.. The 510(k) number is K170022.
When was Klockner Vega TiBase for CEREC approved by the FDA?
Klockner Vega TiBase for CEREC received FDA 510(k) clearance on 2017-11-16, under approval number K170022.
What company makes Klockner Vega TiBase for CEREC?
Klockner Vega TiBase for CEREC is manufactured by SOADCO, S.L..
What is the FDA product code for Klockner Vega TiBase for CEREC?
The FDA product code for Klockner Vega TiBase for CEREC is NHA.
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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.