FDA 510(k) Applications Submitted by Xenco Medical, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K160313 |
02/05/2016 |
Xenco Medical Cervical Interbody System |
XENCO MEDICAL, LLC |
K170611 |
03/01/2017 |
SETx Pedicle Screw System |
Xenco Medical, LLC |
K160986 |
04/08/2016 |
Xenco Medical Pedicle Screw System |
XENCO MEDICAL, LLC |
K161478 |
05/31/2016 |
Xenco Medical Posterior Cervical System |
Xenco Medical, LLC |
K151733 |
06/26/2015 |
Xenco Medical Pedicle Screw System |
Xenco Medical, LLC |
K152302 |
08/14/2015 |
Xenco Medical Cervical Interbody System (Argus) |
Xenco Medical, LLC |
K152987 |
10/13/2015 |
Xenco Medical Cervical Interbody System, Xenco Medical Lumbar Interbody System |
XENCO MEDICAL, LLC |
K143158 |
11/03/2014 |
Xenco Medical Lumbar Interbody System |
Xenco Medical, LLC |
K173933 |
12/26/2017 |
Sorrento Bioglass Bone Graft Substitute |
Xenco Medical, LLC |
K140786 |
03/31/2014 |
XENCO MEDICAL CERVICAL INTERBODY SYSTEM |
XENCO MEDICAL, LLC |
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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