COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM— 510(k) K123297

Substantially Equivalent

Biomet Manufactuting Corp.

FDA 510(k) clearance K123297 for COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM, Substantially Equivalent on 2012-11-20. Applicant: Biomet Manufactuting Corp..

Clearance details

Applicant: Biomet Manufactuting Corp.
Product code: Code MBF
Advisory panel: Orthopedic
Date received: 2012-10-22
Decision date: 2012-11-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

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Adverse events under product code MBF

product code MBF

Injury: 597
Total: 597

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.