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

510(k) Premarket Notification
  • 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
Device Classification Name Hearing Aid, Bone Conduction, Implanted
510(k) Number K182116
Device Name BA310 Abutment, BIA310 Implant/Abutment
Applicant
Cochlear Americas
13059 E Peakview Ave.
Centennial,  CO  80111
Applicant Contact Beth Murray
Correspondent
Cochlear Americas
13059 E Peakview Ave.
Centennial,  CO  80111
Correspondent Contact Beth Murray
Regulation Number874.3302
Classification Product Code
MAH  
Date Received08/06/2018
Decision Date 12/19/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-