COMPREHENSIVE SEGMENTAL REVISION SYSTEM (SRS)— 510(k) K111746

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K111746 for COMPREHENSIVE SEGMENTAL REVISION SYSTEM (SRS), Substantially Equivalent on 2011-12-15. Applicant: Biomet, Inc..

Clearance details

Applicant: Biomet, Inc.
Product code: Code KWT
Advisory panel: Orthopedic
Date received: 2011-06-21
Decision date: 2011-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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Adverse events under product code KWT

product code KWT

Injury: 2,467
Other: 2
Total: 2,469

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.