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) | Registration & Listing | Adverse Events | Recalls | PMA | 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.
 
Trade NameHIRESOLUTION BIONIC EAR SYSTEM
Classification Nameimplant, cochlear
Generic Namecochlear implant
ApplicantADVANCED BIONICS CORP.
PMA NumberP960058
Supplement NumberS043
Date Received07/12/2005
Decision Date12/23/2005
Product Code
MCM[ Registered Establishments with MCM ]
Advisory Committee Ear Nose & Throat
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for process control improvements to the hires90k coil-case/electrode subassembly final molding process. The proposed changes include an external thermocouple to provide closed-loop control of the mold temperature, thereby providing better control of the curing temperature of the silicone, and by configuring the mold tool with spring washer (belleville washers) to allow for smoother movement. The device, as modified, will be marketed under the trade name hiresolution bionic ear system and is indicated for individuals aged 12 months and older with severe-to-profound sensorineural hearing loss to restore a level of auditory sensation via electrical stimulation of the auditory nerve.
-
-