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 Plate, Fixation, Bone
510(k) Number K022230
Device Name NORMED MINI EXTERNAL FIXATOR SYSTEM
Applicant
Osteomedics, Inc.
809 Carter Ln.
Paramus,  NJ  07652
Applicant Contact ALBERT ENAYATI
Correspondent
Osteomedics, Inc.
809 Carter Ln.
Paramus,  NJ  07652
Correspondent Contact ALBERT ENAYATI
Regulation Number888.3030
Classification Product Code
HRS  
Date Received07/10/2002
Decision Date 09/10/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-