FDA 510(k), K083020, STRYKER SPINE REFLEX TRANSLATIONAL ANTERIOR CERVICAL PLATING SYSTEM

510(K) Number: K083020
Device Name: STRYKER SPINE REFLEX TRANSLATIONAL ANTERIOR CERVICAL PLATING SYSTEM
Manufacturer: STRYKER CORP.
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 10/09/2008
Decision Date: 03/26/2009
Regulation Medical Specialty: Orthopedic

Total pages: 586
Fully redacted pages: 306
Content pages: 280