# Zimvie Spine (Zimmer Biomet Spine, Inc.)

- Location (FDA's records): Westminister, CO
- FDA decisions: 4 (2023–2024): 4 510(k) clearances
- Product codes: NKB (2), OLO (2)
- 510(k) review time since 2016: median 29 days, against 81 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Zimmer Biomet Spine, Inc.: 3 (https://510kreport.com/company/zimmer-biomet-spine)

## Firms that cite its devices most
- S.M.A.I.O: 2 (https://510kreport.com/company/smaio)
- Highridge Medical, LLC: 1 (https://510kreport.com/company/highridge-medical)

## Its most-cited devices
- K240539: Vital™ Spinal Fixation System (2024), cited by 3
- K230116: Vital™ Spinal Fixation System (2023), cited by 1

## Recent decisions
- K240647: Virage® Navigation System (Apr 5, 2024)
- K240539: Vital™ Spinal Fixation System (Mar 15, 2024)
- K233443: Vital™ Navigation System (Nov 16, 2023)
- K230116: Vital™ Spinal Fixation System (Oct 11, 2023)

Source page: https://510kreport.com/company/zimvie-spine-zimmer-biomet-spine