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

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