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FDA 510(k) Applications Submitted by NuVasive Incorporated
FDA 510(k) Number
Submission Date
Device Name
Applicant
K193506
12/18/2019
NuVasive X-Core Expandable VBR System, NuVasive X-Core Mini Cervical Expandable VBR System
NuVasive Incorporated
K161442
05/25/2016
NuVasive« CoRoent« Small InterlockÖ System
NUVASIVE INCORPORATED
K152943
10/05/2015
NuVasive Foundation-LL System
NUVASIVE INCORPORATED
K163230
11/17/2016
NuVasive Modulus XLIF Interbody System
NUVASIVE INCORPORATED
K153627
12/18/2015
NuVasive« TLX Interbody System
NUVASIVE INCORPORATED
K162313
08/18/2016
NuVasive Next Generation NVM5 System
NUVASIVE INCORPORATED
K152942
10/05/2015
NuVasiveNVM5 System
NUVASIVE INCORPORATED
K143684
12/24/2014
NuVasive Reline System
NUVASIVE INCORPORATED
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