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FDA 510(k) K083020, STRYKER SPINE REFLEX TRANSLATIONAL ANTERIOR CERVICAL PLATING SYSTEM, by Stryker Corp.

FDA 510(k) K083020, STRYKER SPINE REFLEX TRANSLATIONAL ANTERIOR CERVICAL PLATING SYSTEM, by Stryker Corp.

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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
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