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FDA 510(k), K892059, FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
FDA 510(k), K892059, FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
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510(K) Number: K892059
Device Name: FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
Manufacturer: PROTEK, INC.
Device Classification Name: prosthesis, hip, hemi-, femoral, metal ball
Regulation Number: 888.3360
Classification Product Code: LZY
Date Received: 03/29/1989
Decision Date: 07/19/1989
Regulation Medical Specialty: Orthopedic
Device Name: FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
Manufacturer: PROTEK, INC.
Device Classification Name: prosthesis, hip, hemi-, femoral, metal ball
Regulation Number: 888.3360
Classification Product Code: LZY
Date Received: 03/29/1989
Decision Date: 07/19/1989
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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