FDA 510(k) Applications Submitted by DAVID FAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K230872 |
03/30/2023 |
HalisÖ Lumbar Cage System, LydiaÖ Anterior Lumbar Fusion System, DicaÖ Direction Changeable Lumbar Cage System, KEYSTONE Cage System |
Shanghai Sanyou Medical Co, LTD |
| K230961 |
04/05/2023 |
Zeus Spinal System |
Shanghai Sanyou Medical Co, LTD |
| K211689 |
06/02/2021 |
KEYSTONE PEEK Cage System |
Shanghai Sanyou Medical Co, LTD |
| K231931 |
06/30/2023 |
Adena-Zina Spinal System |
Shanghai Sanyou Medical Co, LTD |
| K212066 |
07/02/2021 |
Adena-Zina System |
Shanghai Sanyou Medical Co, LTD |
| K152781 |
09/25/2015 |
Adena-Zina System |
SHANGHAI SANYOU MEDICAL CO, LTD |
| K163366 |
11/30/2016 |
Shanghai Sanyou CARMEN Cervical Fusion System |
Shanghai Sanyou Medical Co, LTD |
| K163422 |
12/06/2016 |
Shanghai Sanyou PEEK Cage System |
SHANGHAI SANYOU MEDICAL CO, LTD |
| K970361 |
01/31/1997 |
LASER EYE GOGGLES |
STEFANOVSKY & ASSOC. |
|
|
