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 Bone Grafting Material, Synthetic
510(k) Number K843154
Device Name TOOTH ROOT SOCKET GAUGE
Applicant
INTERPORE INTL.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
INTERPORE INTL.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number872.3930
Classification Product Code
LYC  
Date Received08/10/1984
Decision Date 10/01/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-