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FDA 510(k), K842233, NEW JERSEY FEMORAL RESURFACING COMPONENT
FDA 510(k), K842233, NEW JERSEY FEMORAL RESURFACING COMPONENT
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510(K) Number: K842233
Device Name: NEW JERSEY FEMORAL RESURFACING COMPONENT
Manufacturer: ENDOMEDICS, INC.
Device Classification Name: prosthesis, hip, femoral, resurfacing
Regulation Number: 888.3400
Classification Product Code: KXA
Date Received: 06/05/1984
Decision Date: 07/20/1984
Regulation Medical Specialty: Orthopedic
Device Name: NEW JERSEY FEMORAL RESURFACING COMPONENT
Manufacturer: ENDOMEDICS, INC.
Device Classification Name: prosthesis, hip, femoral, resurfacing
Regulation Number: 888.3400
Classification Product Code: KXA
Date Received: 06/05/1984
Decision Date: 07/20/1984
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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