VERTICALE Navigation Instruments
K-Number: K212007 · 2021-08-12
ApplicantSilony Medical GmbH
Decision Date2021-08-12
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
VERTICALE Navigation Instruments is a medical device manufactured by Silony Medical GmbH. It received FDA 510(k) clearance on 2021-08-12 under approval number K212007. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VERTICALE Navigation Instruments?
VERTICALE Navigation Instruments is a medical device that received FDA 510(k) clearance on 2021-08-12. It is manufactured by Silony Medical GmbH. The 510(k) number is K212007.
When was VERTICALE Navigation Instruments approved by the FDA?
VERTICALE Navigation Instruments received FDA 510(k) clearance on 2021-08-12, under approval number K212007.
What company makes VERTICALE Navigation Instruments?
VERTICALE Navigation Instruments is manufactured by Silony Medical GmbH.
What is the FDA product code for VERTICALE Navigation Instruments?
The FDA product code for VERTICALE Navigation Instruments is OLO.
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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.