COAXIAL APPLICATOR SYSTEM— 510(k) K091722

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K091722 for COAXIAL APPLICATOR SYSTEM, Substantially Equivalent on 2010-03-12. Applicant: Biomet, Inc..

Clearance details

Applicant: Biomet, Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 2009-06-11
Decision date: 2010-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.