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 K880737
Device Name SELF GUIDING (SG) INTERLOCKING NAIL
Applicant
Orthopaedic Designs, Inc.
4600 King St. Suite 6e
Alexandria,  VA  22302
Applicant Contact AZAR, M.D.
Correspondent
Orthopaedic Designs, Inc.
4600 King St. Suite 6e
Alexandria,  VA  22302
Correspondent Contact AZAR, M.D.
Regulation Number888.3020
Classification Product Code
HSB  
Date Received02/24/1988
Decision Date 03/14/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-