REVERE 4.5 STABILIZATION SYSTEM— 510(k) K113395

Unknown

Globus Medical, Inc.

FDA 510(k) clearance K113395 for REVERE 4.5 STABILIZATION SYSTEM, Unknown on 2012-06-14. Applicant: Globus Medical, Inc..

Clearance details

Applicant: Globus Medical, Inc.
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2011-11-17
Decision date: 2012-06-14
Decision: Unknown
Clearance type: Traditional
Location: Audubon, PA, 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.