Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Vitality® Spinal Fixation System

K-Number: K203507 · 2021-01-28

Decision Date2021-01-28
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Vitality® Spinal Fixation 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 2021-01-28 under 510(k) number K203507. 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 2021-01-28. The listed applicant is Zimmer Biomet Spine, Inc.. The 510(k) number is K203507.

When did Vitality® Spinal Fixation System receive FDA 510(k) clearance?

Vitality® Spinal Fixation System received FDA 510(k) clearance on 2021-01-28, under 510(k) number K203507.

Who is the listed applicant for Vitality® Spinal Fixation 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 Vitality® Spinal Fixation System?

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

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: NKB)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.