FDA 510(k) Applications Submitted by Gustavo R Prado
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 |
K201085 |
04/23/2020 |
NeVa PV Thrombectomy Device |
Vesalio |
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 |
K141429 |
05/30/2014 |
SORRENTO BONE GRAFT SUBSTITUTE |
HAIDER BIOLOGICS, LLC |
K223563 |
11/29/2022 |
OsteoCNX |
Converg Engineering |
K180373 |
02/12/2018 |
CancelleX Porous Titanium Lumbar Interbody Device |
Xenco Medical, LLC. |
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