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FDA 510(k) K051665, SYNTHES VECTRA-T SYSTEM, by Synthes Spine

FDA 510(k) K051665, SYNTHES VECTRA-T SYSTEM, by Synthes Spine

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510(K) Number: K051665
Device Name: SYNTHES VECTRA-T SYSTEM
Manufacturer: Synthes Spine
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 06/22/2005
Decision Date: 09/09/2005
Regulation Medical Specialty: Orthopedic

Total pages: 98
Fully redacted pages: 42
Content pages: 56
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