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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