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FDA 510(k) Applications Submitted by MARTIN YAHIRO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150362
02/12/2015
NuVasive CoRoent Small Interbody System
NuVasive, Incorporated
K180498
02/26/2018
NuVasive Reline Fenestrated Screws, High V+ Bone Cement
NuVasive, Incorporated
K180550
03/01/2018
NuVasive Monolith Cervical Corpectomy System
NuVasive, Incorporated
K161230
05/02/2016
NuVasive Lumbar Interbody Implants
NUVASIVE, INCORPORATED
K163491
12/12/2016
NuVasive CoRoent Small Interbody System
NuVasive, Incorporated
K153782
12/31/2015
NuVasive« Lumbar Interbody Implants
NUVASIVE, INCORPORATED
K151472
06/01/2015
NuVasive CoRoent Lumbar System
NuVasive, Incorporated
K973560
09/19/1997
BONE GRAFT HARVESTER
DS MFG., INC.
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