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 Retractor, Self-Retaining, For Neurosurgery
510(k) Number K873691
Device Name CEDAR(TM) RETRACTOR RING
Applicant
Cedar Surgical, Inc.
15265 Minnetonka Blvd.
Minnetonka,  MN  55345
Applicant Contact TERRY P CORBIN
Correspondent
Cedar Surgical, Inc.
15265 Minnetonka Blvd.
Minnetonka,  MN  55345
Correspondent Contact TERRY P CORBIN
Regulation Number882.4800
Classification Product Code
GZT  
Date Received09/08/1987
Decision Date 09/28/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-