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 Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
510(k) Number K984357
Device Name TRANSFX EXTERNAL FIXATION SYSTEM
Applicant
IMMEDICA, INC.
100 PASSAIC AVE.
CHATHAM,  NJ  07928 -2848
Applicant Contact ROY BOGERT
Correspondent
IMMEDICA, INC.
100 PASSAIC AVE.
CHATHAM,  NJ  07928 -2848
Correspondent Contact ROY BOGERT
Regulation Number888.3030
Classification Product Code
LXT  
Subsequent Product Codes
JDW   KTT  
Date Received12/07/1998
Decision Date 03/04/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-