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FDA 510(k), K071176, MODIFICATION TO: ARTHREX INTERFERENCE SCREW
FDA 510(k), K071176, MODIFICATION TO: ARTHREX INTERFERENCE SCREW
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510(K) Number: K071176
Device Name: MODIFICATION TO: ARTHREX INTERFERENCE SCREW
Manufacturer: ARTHREX, INC.
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 04/27/2007
Decision Date: 08/03/2007
Regulation Medical Specialty: Orthopedic
Device Name: MODIFICATION TO: ARTHREX INTERFERENCE SCREW
Manufacturer: ARTHREX, INC.
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 04/27/2007
Decision Date: 08/03/2007
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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