• 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 neurological stereotaxic instrument
510(k) Number K030552
Device Name IMAGELESS KNEE MODULE FOR THE STEALTHSTATION SYSTEM
Applicant
MEDTRONIC SURGICAL NAVIGATION TECHNOLOGIES
826 Coal Creek Circle
Louisville,  CO  80027
Applicant Contact VICTORIA G RENDON
Correspondent
MEDTRONIC SURGICAL NAVIGATION TECHNOLOGIES
826 Coal Creek Circle
Louisville,  CO  80027
Correspondent Contact VICTORIA G RENDON
Regulation Number882.4560
Classification Product Code
HAW  
Date Received02/21/2003
Decision Date 03/19/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-