Grandio blocs
K-Number: K171200 · 2017-08-10
ApplicantVoco GmbH
Decision Date2017-08-10
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Grandio blocs is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2017-08-10 under approval number K171200. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Grandio blocs?
Grandio blocs is a medical device that received FDA 510(k) clearance on 2017-08-10. It is manufactured by Voco GmbH. The 510(k) number is K171200.
When was Grandio blocs approved by the FDA?
Grandio blocs received FDA 510(k) clearance on 2017-08-10, under approval number K171200.
What company makes Grandio blocs?
Grandio blocs is manufactured by Voco GmbH.
What is the FDA product code for Grandio blocs?
The FDA product code for Grandio blocs is EBF.
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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.