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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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