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 System, X-Ray, Tomography, Computed
510(k) Number K170023
Device Name SPiN Thoracic Navigation System
Applicant
Veran Medical Technologies, Inc.
1908 Innerbelt Business Center Dr
St. Louis,  MO  63114
Applicant Contact Scott Wrightstone
Correspondent
Veran Medical Technologies, Inc.
1908 Innerbelt Business Center Dr
St. Louis,  MO  63114
Correspondent Contact Scott Wrightstone
Regulation Number892.1750
Classification Product Code
JAK  
Date Received01/03/2017
Decision Date 05/15/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-