• 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 K141211
Device Name INCLUSIVE TITANIUM ABUTMENTS COMPATIBLE WITH STRAUMANN TISSUE LEVEL IMPLANTS
Applicant
PRISMATIK DENTALCRAFT, INC.
2212 DUPONT DRIVE, SUITE P
IRVINE,  CA  92612
Applicant Contact Armin Zehtabchi
Correspondent
PRISMATIK DENTALCRAFT, INC.
2212 DUPONT DRIVE, SUITE P
IRVINE,  CA  92612
Correspondent Contact Armin Zehtabchi
Regulation Number872.3630
Classification Product Code
NHA  
Date Received05/09/2014
Decision Date 10/22/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-