S Cervical Occipital Plating System

Aesculap Implant Systems, LLC Receives FDA 510(k) Clearance for the S4 Cervical Occipital Plating System

Center Valley, PA (September 9, 2010) – The Aesculap Implant Systems S4 Cervical Occipital Plating System has been cleared for marketing by the FDA under K100147.  The agency began review of the Special 510(k) on January 19, 2010 and received the Substantial Equivalence determination on July 23, 2010. The S4 Cervical Occipital Plating System is used to promote spinal fusion of the cervical and thoracic spine (C1-T3) and occipito-cervico-thoracic junction (occiput-T3) in patients with degenerative disease or fracture.

Contact:
John Gotzon
Product Manager
Aesculap Implant Systems, LLC
1-800-234-9179
john.gotzon@aesculap.com 

 
 

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