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FDA 510(k), K070978, ZIMMER SEGMENTAL SYSTEM
FDA 510(k), K070978, ZIMMER SEGMENTAL SYSTEM
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510(K) Number: K070978
Device Name: ZIMMER SEGMENTAL SYSTEM
Manufacturer: ZIMMER, INC.
Device Classification Name: prosthesis, knee, femorotibial, constrained, cemented, metal/polymer
Regulation Number: 888.3510
Classification Product Code: KRO
Date Received: 04/06/2007
Decision Date: 07/03/2007
Regulation Medical Specialty: Orthopedic
Device Name: ZIMMER SEGMENTAL SYSTEM
Manufacturer: ZIMMER, INC.
Device Classification Name: prosthesis, knee, femorotibial, constrained, cemented, metal/polymer
Regulation Number: 888.3510
Classification Product Code: KRO
Date Received: 04/06/2007
Decision Date: 07/03/2007
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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