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FDA 510(k), K041393, FASSIER-DUVAL TELSCOPIC IM SYSTEM
FDA 510(k), K041393, FASSIER-DUVAL TELSCOPIC IM SYSTEM
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510(K) Number: K041393
Device Name: FASSIER-DUVAL TELSCOPIC IM SYSTEM
Manufacturer: PEGA MEDICAL INC.
Device Classification Name: rod, fixation, intramedullary and accessories
Regulation Number: 888.3020
Classification Product Code: HSB
Date Received: 05/24/2004
Decision Date: 08/17/2004
Regulation Medical Specialty: Orthopedic
Device Name: FASSIER-DUVAL TELSCOPIC IM SYSTEM
Manufacturer: PEGA MEDICAL INC.
Device Classification Name: rod, fixation, intramedullary and accessories
Regulation Number: 888.3020
Classification Product Code: HSB
Date Received: 05/24/2004
Decision Date: 08/17/2004
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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