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FDA 510(k)

Vitality® Spinal Fixation System

K-Number: K183550 · 2019-04-08

ApplicantZimmer Biomet Spine, Inc.
Decision Date2019-04-08
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Vitality® Spinal Fixation System is a medical device manufactured by Zimmer Biomet Spine, Inc.. It received FDA 510(k) clearance on 2019-04-08 under approval number K183550. 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 Vitality® Spinal Fixation System?

Vitality® Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2019-04-08. It is manufactured by Zimmer Biomet Spine, Inc.. The 510(k) number is K183550.

When was Vitality® Spinal Fixation System approved by the FDA?

Vitality® Spinal Fixation System received FDA 510(k) clearance on 2019-04-08, under approval number K183550.

What company makes Vitality® Spinal Fixation System?

Vitality® Spinal Fixation System is manufactured by Zimmer Biomet Spine, Inc..

What is the FDA product code for Vitality® Spinal Fixation System?

The FDA product code for Vitality® Spinal Fixation System is NKB.

Related Clinical Trials

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Related PubMed Literature

PMID: 41612341 Brain-computer interface commercialization. Journal of neuroengineering and rehabilitation (2026) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by Zimmer Biomet Spine, Inc.

K172275Vitality® Spinal Fixation System, Vitality®+ Power Instrument System K171907Vitality® Spinal Fixation System K163543Biomet Fusion System K180227Polaris Spinal Growth System K171495Zyston Strut Open Titanium Spacer System K191722Vital Navigation System

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Related Devices (Code: NKB)

K163301CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc. K162134ENNOVATE Spinal SystemAesculap Implant Systems, LLC K162912VIPER PRIME™ additions to the VIPER® SystemMedos International SARL K162160Preference Elite Pedicle Screw SystemAmedica Corporation K162232MOSS 100 Pedicle Screw SystemBiedermann Motech GmbH & Co. KG K162379CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc.

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.

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