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 Rod, Fixation, Intramedullary And Accessories
510(k) Number K981230
Device Name ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
Applicant
BIODYNAMIC TECHNOLOGIES, INC.
1425 EAST NEWPORT CENTER DR.
DEERFIELD BEACH,  FL  33442
Applicant Contact DANNY HODGEMAN
Correspondent
BIODYNAMIC TECHNOLOGIES, INC.
1425 EAST NEWPORT CENTER DR.
DEERFIELD BEACH,  FL  33442
Correspondent Contact DANNY HODGEMAN
Regulation Number888.3020
Classification Product Code
HSB  
Date Received04/03/1998
Decision Date 06/01/1998
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
-
-