Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 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.
 
DeviceNEUROCONTROL FREEHAND SYSTEM
Generic NameStimulator, neuromuscular, implanted
Regulation Number882.5860
ApplicantBIOCONTROL TECHNOLOGY, INC.
1945 EAST 97TH
CLEVELAND, OH 44106-4720
PMA NumberP950035
Supplement NumberS006
Date Received02/29/2000
Decision Date07/05/2000
Product Code GZC 
Advisory Committee Ear Nose & Throat
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL FOR THE DISTRIBUTION OF AN INTRAMUSCULAR ELECTRODE AND INTRAMUSCULAR ELECTRODE INSERTION TOOL KIT AS COMPONENTS TO THE FREEHAND(TM) SYSTEM, AND LABELING CHANGES.
-
-