FDA 510(k) Applications Submitted by Anthony DeBenedictis
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K190122 |
01/25/2019 |
Renovis A200 PS Knee System as part of the Renovis A200 Knee System |
Renovis Surgical Technologies |
| K200328 |
02/10/2020 |
Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System |
Kyocera Medical Technologies, Inc. |
| K180502 |
02/26/2018 |
S128 Anterior Lumbar Interbody Fusion (ALIF) System |
Renovis Surgical Technologies Inc. |
| K200709 |
03/18/2020 |
Kyocera Bipolar Hip System |
Kyocera Medical Technologies, Inc. |
| K170888 |
03/27/2017 |
Renovis S141 Lumbar Interbody Fusion System |
Renovis Surgical Technologies |
| K171543 |
05/26/2017 |
Renovis Surgical Hip Replacement System |
Renovis Surgical Technologies |
| K201660 |
06/18/2020 |
KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System |
Kyocera Medical Technologies, Inc. |
| K181655 |
06/22/2018 |
Renovis S180 Lateral Lumbar Interbody Fusion System |
Renovis Surgical Technologies |
| K212070 |
07/02/2021 |
KMTI S141 Lumbar Interbody Fusion System |
Kyocera Medical Technologies, Inc. |
| K182007 |
07/27/2018 |
Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System |
Renovis Surgical Technologies |
| K152193 |
08/05/2015 |
Renovis Anterior Cervical Plate System |
Renovis Surgical Technologies, Inc. |
| K153250 |
11/09/2015 |
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System |
RENOVIS SURGICAL TECHNOLOGIES |
| K203472 |
11/25/2020 |
KMTI Hip Replacement System |
Kyocera Medical Technologies, Inc. |
| K193320 |
12/02/2019 |
KMTI Tesera SA Anterior Lumbar Interbody Fusion (ALIF) System |
Kyocera Medical Technologies, Inc. |
| K143647 |
12/22/2014 |
Renovis Surgical Hip Replacement System |
Renovis Surgical Technologies, Inc. |
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