FDA 510(k), K110397, TRUMATCH PERSONALIZED SOLUTIONS
FDA 510(k), K110397, TRUMATCH PERSONALIZED SOLUTIONS
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$149.00 USD
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510(K) Number: K110397
Device Name: TRUMATCH PERSONALIZED SOLUTIONS
Manufacturer:
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: 888.3560
Classification Product Code: JWH
Date Received: 02/11/2011
Decision Date: 08/16/2011
Regulation Medical Specialty: Orthopedic
Device Name: TRUMATCH PERSONALIZED SOLUTIONS
Manufacturer:
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: 888.3560
Classification Product Code: JWH
Date Received: 02/11/2011
Decision Date: 08/16/2011
Regulation Medical Specialty: Orthopedic