• 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 Orthopedic Stereotaxic Instrument
510(k) Number K143668
Device Name Navio
Applicant
Blue Belt Technologies, Inc.
2828 Liberty Ave.
Suite 100
Pittsburgh,  PA  15222
Applicant Contact RICHARD G CONFER
Correspondent
Blue Belt Technologies, Inc.
2828 Liberty Ave.
Suite 100
Pittsburgh,  PA  15222
Correspondent Contact RICHARD G CONFER
Regulation Number882.4560
Classification Product Code
OLO  
Subsequent Product Codes
HRY   HSX   KRR   NPJ  
Date Received12/24/2014
Decision Date 03/20/2015
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-