ATR 5000, LC 5000, IMPLANT SYSTEM— 510(k) K033597

Name: FDA 510(k) clearance K033597
Creator: U.S. Food and Drug Administration
Published: 2003-11-25

Substantially Equivalent

Advanced Technology Research (A.T.R.) S.R.L.

FDA 510(k) clearance K033597 for ATR 5000, LC 5000, IMPLANT SYSTEM, Substantially Equivalent on 2003-11-25. Applicant: Advanced Technology Research (A.T.R.) S.R.L.. Device class: 1.

Clearance details

Applicant: Advanced Technology Research (A.T.R.) S.R.L.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2003-11-14
Decision date: 2003-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pistoia, IT

Download summary PDF View on FDA.gov ↗

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