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 Surgical Table Cushion
510(k) Number K873690
Device Name CEDAR(TM) PELVIC CUSHION
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 Number878.4950
Classification Product Code
LWG  
Date Received09/08/1987
Decision Date 10/26/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-