ARTHREX GRAFT HARVESTING KIT— 510(k) K941285

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K941285 for ARTHREX GRAFT HARVESTING KIT, Substantially Equivalent on 1994-11-14. Applicant: Arthrex, Inc.. Device class: 1.

Clearance details

Applicant: Arthrex, Inc.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1994-03-17
Decision date: 1994-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.