1-CUT ACL GRAFT KNIFE— 510(k) K905380

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K905380 for 1-CUT ACL GRAFT KNIFE, Substantially Equivalent on 1990-12-13. Applicant: Depuy, Inc.. Device class: 1.

Clearance details

Applicant: Depuy, Inc.
Product code: Code GDX
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1990-11-30
Decision date: 1990-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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