Vertera Spine Cohere Cervical Interbody Fusion Device— 510(k) K173030

Substantially Equivalent

Nu Vasive, Incorporated

FDA 510(k) clearance K173030 for Vertera Spine Cohere Cervical Interbody Fusion Device, Substantially Equivalent on 2017-11-21. Applicant: Nu Vasive, Incorporated.

Clearance details

Applicant: Nu Vasive, Incorporated
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2017-09-28
Decision date: 2017-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.