• 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 K983347
Device Name OSSEOTITE DENTAL IMPLANTS
Applicant
Implant Innovations, Inc.
4555 Riverside Dr.
Palm Beach Gardens,  FL  33410
Applicant Contact WILLIAM G CONETY
Correspondent
Implant Innovations, Inc.
4555 Riverside Dr.
Palm Beach Gardens,  FL  33410
Correspondent Contact WILLIAM G CONETY
Regulation Number872.3640
Classification Product Code
DZE  
Date Received09/23/1998
Decision Date 01/06/1999
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
-
-