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FDA 510(k), K030625, SPINAL CONCEPTS INC. PATHFINDER
FDA 510(k), K030625, SPINAL CONCEPTS INC. PATHFINDER
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510(K) Number: K030625
Device Name: SPINAL CONCEPTS INC. PATHFINDER
Manufacturer: SPINAL CONCEPTS, INC.
Device Classification Name: thoracolumbosacral pedicle screw system
Regulation Number: 888.3070
Classification Product Code: NKB
Date Received: 02/27/2003
Decision Date: 03/28/2003
Regulation Medical Specialty: Orthopedic
Device Name: SPINAL CONCEPTS INC. PATHFINDER
Manufacturer: SPINAL CONCEPTS, INC.
Device Classification Name: thoracolumbosacral pedicle screw system
Regulation Number: 888.3070
Classification Product Code: NKB
Date Received: 02/27/2003
Decision Date: 03/28/2003
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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