Vitality® Spinal Fixation System— 510(k) K183550

Substantially Equivalent

Zimmer Biomet Spine, Inc.

FDA 510(k) clearance K183550 for Vitality® Spinal Fixation System, Substantially Equivalent on 2019-04-08. Applicant: Zimmer Biomet Spine, Inc..

Clearance details

Applicant: Zimmer Biomet Spine, Inc.
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2018-12-20
Decision date: 2019-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westminister, CO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NKB

product code NKB

Death: 27
Injury: 5,033
Malfunction: 4,140
Total: 9,200

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.