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FDA 510(k), K042600, STANSION MATRIX
FDA 510(k), K042600, STANSION MATRIX
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510(K) Number: K042600
Device Name: STANSION MATRIX
Manufacturer: SPINEWORKS, LLC
Device Classification Name: Spinal Vertebral Body Replacement Device
Regulation Number: 888.3060
Classification Product Code: MQP
Date Received: 09/23/2004
Decision Date: 02/18/2005
Regulation Medical Specialty: Orthopedic
Device Name: STANSION MATRIX
Manufacturer: SPINEWORKS, LLC
Device Classification Name: Spinal Vertebral Body Replacement Device
Regulation Number: 888.3060
Classification Product Code: MQP
Date Received: 09/23/2004
Decision Date: 02/18/2005
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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