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FDA 510(k), K130126, SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM
FDA 510(k), K130126, SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K130126
Device Name: SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM
Manufacturer:
Device Classification Name: Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
Regulation Number: 888.3670
Classification Product Code: MBF
Date Received: 01/17/2013
Decision Date: 08/06/2013
Regulation Medical Specialty: Orthopedic
Device Name: SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM
Manufacturer:
Device Classification Name: Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
Regulation Number: 888.3670
Classification Product Code: MBF
Date Received: 01/17/2013
Decision Date: 08/06/2013
Regulation Medical Specialty: Orthopedic
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