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FDA 510(k)

Vital™ Spinal Fixation System

K-Number: K230116 · 2023-10-11

Decision Date2023-10-11
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Vital™ Spinal Fixation System is a medical device manufactured by Zimvie Spine (Zimmer Biomet Spine, Inc.). It received FDA 510(k) clearance on 2023-10-11 under approval number K230116. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vital™ Spinal Fixation System?

Vital™ Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2023-10-11. It is manufactured by Zimvie Spine (Zimmer Biomet Spine, Inc.). The 510(k) number is K230116.

When was Vital™ Spinal Fixation System approved by the FDA?

Vital™ Spinal Fixation System received FDA 510(k) clearance on 2023-10-11, under approval number K230116.

What company makes Vital™ Spinal Fixation System?

Vital™ Spinal Fixation System is manufactured by Zimvie Spine (Zimmer Biomet Spine, Inc.).

What is the FDA product code for Vital™ Spinal Fixation System?

The FDA product code for Vital™ Spinal Fixation System is NKB.

Related Clinical Trials

Related PubMed Literature

Other Devices by Zimvie Spine (Zimmer Biomet Spine, Inc.)

Related Devices (Code: NKB)

Official Source

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