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FDA 510(k), K062466, ARTHREX INTERFERENCE SCREW
FDA 510(k), K062466, ARTHREX INTERFERENCE SCREW
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510(K) Number: K062466
Device Name: ARTHREX INTERFERENCE SCREW
Manufacturer: ARTHREX, INC.
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 08/24/2006
Decision Date: 11/29/2006
Regulation Medical Specialty: Orthopedic
Device Name: ARTHREX INTERFERENCE SCREW
Manufacturer: ARTHREX, INC.
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 08/24/2006
Decision Date: 11/29/2006
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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