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 K201700
Device Name BEGO Semados® RS/RSX Implant System
Applicant
Bego Implant Systems GmbH & Co. KG
Wilhelm-Herbst-Str. 1
Bremen,  DE 28359
Applicant Contact Bertrand Lecointe
Correspondent
Bego Implant Systems GmbH & Co. KG
Wilhelm-Herbst-Str. 1
Bremen,  DE 28359
Correspondent Contact Bertrand Lecointe
Regulation Number872.3640
Classification Product Code
DZE  
Subsequent Product Code
NHA  
Date Received06/22/2020
Decision Date 01/13/2021
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
-
-