Vitality® Spinal Fixation System
K-Number: K171907 · 2017-07-14
ApplicantZimmer Biomet Spine, Inc.
Decision Date2017-07-14
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 2017-07-14 under approval number K171907. 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 2017-07-14. It is manufactured by Zimmer Biomet Spine, Inc.. The 510(k) number is K171907.
When was Vitality® Spinal Fixation System approved by the FDA?
Vitality® Spinal Fixation System received FDA 510(k) clearance on 2017-07-14, under approval number K171907.
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.
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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.