• 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 Drills, Burrs, Trephines & Accessories (Manual)
510(k) Number K122456
Device Name MRII CRAINIAL DRILL
Applicant
MRI INTERVENTIONS, INC.
5 MUSICK
IRVINE,  CA  92618
Applicant Contact E.F. WADDELL
Correspondent
MRI INTERVENTIONS, INC.
5 MUSICK
IRVINE,  CA  92618
Correspondent Contact E.F. WADDELL
Regulation Number882.4300
Classification Product Code
HBG  
Date Received08/13/2012
Decision Date 03/22/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-