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FDA 510(k), K771708, WORRELL PATELLA
FDA 510(k), K771708, WORRELL PATELLA
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510(K) Number: K771708
Device Name: WORRELL PATELLA
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Regulation Number: HTG
Classification Product Code: 09/12/1977
Date Received: 10/06/1977
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: WORRELL PATELLA
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Regulation Number: HTG
Classification Product Code: 09/12/1977
Date Received: 10/06/1977
Decision Date: Substantially Equivalent (SESE)
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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