FDA 510(k), K950709, SYNERGY TI ANTERIOR SPINAL SYSTEM

FDA 510(k), K950709, SYNERGY TI ANTERIOR SPINAL SYSTEM

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510(K) Number: K950709
Device Name: SYNERGY TI ANTERIOR SPINAL SYSTEM
Manufacturer: CROSS MEDICAL PRODUCTS, INC.
Device Classification Name: appliance, fixation, spinal intervertebral body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 02/13/1995
Decision Date: 10/25/1995
Regulation Medical Specialty: Orthopedic

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