ARTHREX CHONDRAL DART, MODEL AR-4005B-18— 510(k) K991971

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K991971 for ARTHREX CHONDRAL DART, MODEL AR-4005B-18, Substantially Equivalent on 2000-08-04. Applicant: Arthrex, Inc..

Clearance details

Applicant: Arthrex, Inc.
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 1999-06-11
Decision date: 2000-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.