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FDA 510(k), K000742, SYNTHES ANTERIOR CSLP SYSTEM
FDA 510(k), K000742, SYNTHES ANTERIOR CSLP SYSTEM
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510(K) Number: K000742
Device Name: SYNTHES ANTERIOR CSLP SYSTEM
Manufacturer: SYNTHES SPINE
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 03/07/2000
Decision Date: 03/29/2000
Regulation Medical Specialty: Orthopedic
Device Name: SYNTHES ANTERIOR CSLP SYSTEM
Manufacturer: SYNTHES SPINE
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 03/07/2000
Decision Date: 03/29/2000
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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