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 abutment, implant, dental, endosseous
510(k) Number K052957
Device Name IMPLANTIUM PROSTHETICS
Applicant
DENTIUM CO., LTD.
5536 TROWBRIDGE DRIVE
DUNWOODY,  GA  30338
Applicant Contact CATHRYN N CAMBRIA
Correspondent
DENTIUM CO., LTD.
5536 TROWBRIDGE DRIVE
DUNWOODY,  GA  30338
Correspondent Contact CATHRYN N CAMBRIA
Regulation Number872.3630
Classification Product Code
NHA  
Date Received10/21/2005
Decision Date 07/27/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-