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 Accessories, Traction
510(k) Number K831135
Device Name SAUNDERS #7080 CERVICAL TRACTION SYS
Applicant
Chattanooga Group, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Chattanooga Group, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number890.5925
Classification Product Code
ILZ  
Date Received04/07/1983
Decision Date 06/24/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-