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FDA 510(k)

Vital Navigation System

K-Number: K191722 · 2019-12-02

Decision Date2019-12-02
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Vital Navigation System is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Biomet Spine, Inc.. It received FDA 510(k) clearance on 2019-12-02 under 510(k) 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. The listed applicant is Zimmer Biomet Spine, Inc.. The 510(k) number is K191722.

When did Vital Navigation System receive FDA 510(k) clearance?

Vital Navigation System received FDA 510(k) clearance on 2019-12-02, under 510(k) number K191722.

Who is the listed applicant for Vital Navigation System?

The FDA 510(k) record lists Zimmer Biomet Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vital Navigation System?

The FDA product code for Vital Navigation System is OLO.

Other records listing Zimmer Biomet Spine, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 15 devices →

Related Devices (Code: OLO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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