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FDA 510(k) Applications Submitted by Jason Haider
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190364
02/15/2019
CancelleX Porous Titanium Lumbar Interbody Device
Xenco Medical, LLC
K191074
04/23/2019
Sorrento Bone Graft Substitute
Xenco Medical, LLC
K223059
09/30/2022
Xenco Medical InterAlign Cervical Interbody System
Xenco Medical, LLC
K213456
10/26/2021
Xenco Medical Multilevel CerviKit
Xenco Medical, LLC
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