510(k) K032507— INTERLOK BIO-MODULAR HUMERAL STEMS

Substantially Equivalent

Biomet, Inc.

Clearance details

Applicant: Biomet, Inc.
Product code: Code KWT
Advisory panel: Orthopedic
Date received: 2003-08-14
Decision date: 2003-09-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

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.