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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceSuperion Indirect Decompression System
Generic NameProsthesis, spinous process spacer/plate
ApplicantBoston Scientific Neuromodulation
25155 Rye Canyon Loop
Valencia, CA 91355
PMA NumberP140004
Supplement NumberS008
Date Received02/21/2017
Decision Date06/07/2017
Product Code NQO 
Advisory Committee Orthopedic
Supplement TypeNormal 180 Day Track No User Fee
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for a manufacturing site located at Turner Medical, Inc., 130 Durham Drive, Athens, Alabama for the production of the Superion InterSpinous Decompression System.
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