FDA 510(k), K131283, PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES
FDA 510(k), K131283, PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES
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510(K) Number: K131283
Device Name: PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES
Manufacturer:
Device Classification Name: Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
Regulation Number: 888.3110
Classification Product Code: HSN
Date Received: 05/06/2013
Decision Date: 07/05/2013
Regulation Medical Specialty: Orthopedic
Device Name: PROPHECY INFINITY PREOPERATIVE NAVIGATION ALIGNMENT GUIDES
Manufacturer:
Device Classification Name: Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
Regulation Number: 888.3110
Classification Product Code: HSN
Date Received: 05/06/2013
Decision Date: 07/05/2013
Regulation Medical Specialty: Orthopedic