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FDA 510(k) K094041, ALPHA ORTHOPAEDICS AT3 SYSTEM, by Alpha Orthopaedics

FDA 510(k) K094041, ALPHA ORTHOPAEDICS AT3 SYSTEM, by Alpha Orthopaedics

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510(K) Number: K094041
Device Name: ALPHA ORTHOPAEDICS AT3 SYSTEM
Manufacturer: Alpha Orthopaedics
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 12/30/2009
Decision Date: 04/07/2010
Regulation Medical Specialty: General & Plastic Surgery
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