Vital Navigation System
K-Number: K191722 · 2019-12-02
ApplicantZimmer Biomet Spine, Inc.
Decision Date2019-12-02
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Vital Navigation System is a medical device manufactured by Zimmer Biomet Spine, Inc.. It received FDA 510(k) clearance on 2019-12-02 under approval number K191722. 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 Vital Navigation System?
Vital Navigation System is a medical device that received FDA 510(k) clearance on 2019-12-02. It is manufactured by Zimmer Biomet Spine, Inc.. The 510(k) number is K191722.
When was Vital Navigation System approved by the FDA?
Vital Navigation System received FDA 510(k) clearance on 2019-12-02, under approval number K191722.
What company makes Vital Navigation System?
Vital Navigation System is manufactured by Zimmer Biomet Spine, Inc..
What is the FDA product code for Vital Navigation System?
The FDA product code for Vital Navigation System 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.