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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: KXA
Date Received: 01/07/2000
Decision Date: 03/30/2000
Decision: 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: KXA
Date Received: 01/07/2000
Decision Date: 03/30/2000
Decision: Substantially Equivalent (SESE)
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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