• 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 thoracolumbosacral pedicle screw system
510(k) Number K190636
Device Name NuVasive® Reline® 4.5-5.0 System
Applicant
NuVasive, Incorporated
7475 Lusk Boulevard
san diego,  CA  92121
Applicant Contact ivanna lopez
Correspondent
NuVasive, Incorporated
7475 Lusk Boulevard
san diego,  CA  92121
Correspondent Contact ivanna lopez
Regulation Number888.3070
Classification Product Code
NKB  
Subsequent Product Codes
KWP   KWQ  
Date Received03/12/2019
Decision Date 10/19/2019
Decision substantially equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-