FDA 510(k), K000046, KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)
FDA 510(k), K000046, KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)
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510(K) Number: K000046
Device Name: KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)
Manufacturer: ROBERT L CASARSA
Device Classification Name: Arthroscope
Regulation Number: HRX
Classification Product Code: 01/07/2000
Date Received: 03/30/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: KNIGHT ENDOSCOPIC SPINE SYSTEM (KESS)
Manufacturer: ROBERT L CASARSA
Device Classification Name: Arthroscope
Regulation Number: HRX
Classification Product Code: 01/07/2000
Date Received: 03/30/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
- 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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