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 goniometer, nonpowered
510(k) Number K870767
Device Name THE (CROM) TESTER
Applicant
TWIN CITY SURGICAL, INC.
2800 N.FAIRVIEW AVE.
ST. PAUL,  MN  55113
Applicant Contact WAYNE O DUESCHER
Correspondent
TWIN CITY SURGICAL, INC.
2800 N.FAIRVIEW AVE.
ST. PAUL,  MN  55113
Correspondent Contact WAYNE O DUESCHER
Regulation Number888.1520
Classification Product Code
KQW  
Date Received02/26/1987
Decision Date 03/17/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-