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 plate, fixation, bone
510(k) Number K122538
Device Name ACUMED PELVIC BONE PLATE SYSTEM
Applicant
ACUMED LLC
5885 NW Cornelius Pass Rd
HILLSBORO,  OR  97124
Applicant Contact KARA BUDOR
Correspondent
ACUMED LLC
5885 NW Cornelius Pass Rd
HILLSBORO,  OR  97124
Correspondent Contact KARA BUDOR
Regulation Number888.3030
Classification Product Code
HRS  
Date Received08/21/2012
Decision Date 11/19/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-