• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
DeviceSCOLITRON(TM) STIMULATOR
Classification Namestimulator, functional neuromuscular, scoliosis
Generic Namestimulator, functional neuromuscular, scoliosis
Applicant
EBI, L.P.
399 jefferson road
parsippany, NJ 07054
PMA NumberP820008
Supplement NumberS002
Date Received09/03/1985
Decision Date01/17/1986
Product Code
LWB
Advisory Committee Neurology
Expedited Review Granted? No
Combination Product No
-
-