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 K122988
Device Name KLOCKNER DENTAL IMPLANT ABUTMENTS
Applicant
SOADCO, S.L.
AV FITER I ROSSELL
4 BIS LOCAL 2
ESCALDES-ENGORDANY,  AD AD-700
Applicant Contact MARIA MITJANETA
Correspondent
SOADCO, S.L.
AV FITER I ROSSELL
4 BIS LOCAL 2
ESCALDES-ENGORDANY,  AD AD-700
Correspondent Contact MARIA MITJANETA
Regulation Number872.3630
Classification Product Code
NHA  
Date Received09/26/2012
Decision Date 07/19/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
-
-