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FDA 510(k), K800800, PATELLAR COMPONENT FOR LUBINUS PATELLAR
FDA 510(k), K800800, PATELLAR COMPONENT FOR LUBINUS PATELLAR
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510(K) Number: K800800
Device Name: PATELLAR COMPONENT FOR LUBINUS PATELLAR
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Regulation Number: HTG
Classification Product Code: 04/10/1980
Date Received: 04/21/1980
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: PATELLAR COMPONENT FOR LUBINUS PATELLAR
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Regulation Number: HTG
Classification Product Code: 04/10/1980
Date Received: 04/21/1980
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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