ARTHREX INSTRUMENTS (BASIC)— 510(k) K925954

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K925954 for ARTHREX INSTRUMENTS (BASIC), Substantially Equivalent on 1993-03-04. Applicant: Arthrex, Inc..

Clearance details

Applicant: Arthrex, Inc.
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 1992-11-24
Decision date: 1993-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

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Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.