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 Implant, Endosseous, Root-Form
510(k) Number K980630
Device Name FRIALIT-2 CORABASE
Applicant
Friatec AG
One America Plz.
600 W. Broadway, Suite 900
San Diego,  CA  92101
Applicant Contact EUGENE GOORCHENKO
Correspondent
Friatec AG
One America Plz.
600 W. Broadway, Suite 900
San Diego,  CA  92101
Correspondent Contact EUGENE GOORCHENKO
Regulation Number872.3640
Classification Product Code
DZE  
Date Received02/18/1998
Decision Date 09/04/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-