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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.
 
DeviceSPINAL-STIM LITE SPINAL FUSION SYSTEM
Generic NameStimulator, bone growth, non-invasive
Regulation Number890.5870
ApplicantOrthofix, Inc.
3451 Plano Pkwy.
Lewisville, TX 75056
PMA NumberP850007
Supplement NumberS019
Date Received06/12/1996
Decision Date09/19/1997
Reclassified Date05/18/2026
Product Code LOF 
Advisory Committee Orthopedic
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for the Spinal-Stim(R) Lite Spinal Fusion System, Model 212L. The device will be marketed under the trade name Spinal-Stim(R) and is indicated as a spinal fusion adjunct to increase the probability of fusion success ans as a nonooperative treatment for salvage of failed spinal fusion, where a minimum of nine months has elapsed since the last surgery.
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