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FDA 510(k), K960656, GORE BURR HOLE COVER
FDA 510(k), K960656, GORE BURR HOLE COVER
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510(K) Number: K960656
Device Name: GORE BURR HOLE COVER
Manufacturer: W.L. GORE & ASSOCIATES,INC
Device Classification Name: cover, burr hole
Regulation Number: 882.5250
Classification Product Code: GXR
Date Received: 02/15/1996
Decision Date: 08/14/1996
Regulation Medical Specialty: Neurology
Device Name: GORE BURR HOLE COVER
Manufacturer: W.L. GORE & ASSOCIATES,INC
Device Classification Name: cover, burr hole
Regulation Number: 882.5250
Classification Product Code: GXR
Date Received: 02/15/1996
Decision Date: 08/14/1996
Regulation Medical Specialty: Neurology
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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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