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FDA 510(k), K951302, SMALL FRAGMENT PLATES AND SCREWS
FDA 510(k), K951302, SMALL FRAGMENT PLATES AND SCREWS
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510(K) Number: K951302
Device Name: SMALL FRAGMENT PLATES AND SCREWS
Manufacturer: ROB MEDOFF
Device Classification Name: Nail, Fixation, Bone
Regulation Number: JDS
Classification Product Code: 03/22/1995
Date Received: 05/05/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: SMALL FRAGMENT PLATES AND SCREWS
Manufacturer: ROB MEDOFF
Device Classification Name: Nail, Fixation, Bone
Regulation Number: JDS
Classification Product Code: 03/22/1995
Date Received: 05/05/1995
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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