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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 NumberS033
Date Received06/06/2024
Decision Date08/22/2024
Product Code NQO 
Advisory Committee Orthopedic
Supplement TypeNormal 180 Day Track
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
approval to manufacture the Superion IDS Instrument kits (Vertiflex Instrument Platform Kit (VIP Kit) and Single Use Instruments Kit (SUI Kit)) at the following alternate manufacturing site: AUSA Medical Devices (Adroit USA, Inc.)
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