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FDA 510(k), K904879, BEUCHEL-PAPPAS GLENOID COMPONENT
FDA 510(k), K904879, BEUCHEL-PAPPAS GLENOID COMPONENT
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510(K) Number: K904879
Device Name: BEUCHEL-PAPPAS GLENOID COMPONENT
Manufacturer: ENDOTEC, INC.
Device Classification Name: prosthesis, shoulder, semi-constrained, metal/polymer cemented
Regulation Number: 888.3660
Classification Product Code: KWS
Date Received: 10/30/1990
Decision Date: 01/28/1991
Regulation Medical Specialty: Orthopedic
Device Name: BEUCHEL-PAPPAS GLENOID COMPONENT
Manufacturer: ENDOTEC, INC.
Device Classification Name: prosthesis, shoulder, semi-constrained, metal/polymer cemented
Regulation Number: 888.3660
Classification Product Code: KWS
Date Received: 10/30/1990
Decision Date: 01/28/1991
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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