FDA 510(k), K072629, DIGIMATCH ROBODOC SURGICAL SYSTEM

FDA 510(k), K072629, DIGIMATCH ROBODOC SURGICAL SYSTEM

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510(K) Number: K072629
Device Name: DIGIMATCH ROBODOC SURGICAL SYSTEM
Manufacturer:
Device Classification Name: Orthopedic Computer Controlled Surgical System
Regulation Number: 882.4560
Classification Product Code: OJP
Date Received: 09/17/2007
Decision Date: 08/06/2008
Regulation Medical Specialty: Neurology
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