STALIF CTI, STALIF C— 510(k) K142079

Substantially Equivalent

Centinel Spine, Inc.

FDA 510(k) clearance K142079 for STALIF CTI, STALIF C, Substantially Equivalent on 2014-10-24. Applicant: Centinel Spine, Inc..

Clearance details

Applicant: Centinel Spine, Inc.
Product code: Code OVE
Advisory panel: Orthopedic
Date received: 2014-07-31
Decision date: 2014-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OVE

product code OVE

Injury: 293
Malfunction: 710
Total: 1,003

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.