Apollo Endosurgery, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories3
Latest Approval2023-09-18
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K232544 | Apollo ESG NXT System, Apollo REVISE NXT System | QTD | 2023-09-18 | View |
| 510(k) | K231553 | OverStitch NXT Endoscopic Suturing System | OCW | 2023-06-29 | View |
| 510(k) | DEN210045 | APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System | QTD | 2022-07-12 | View |
| 510(k) | K210266 | OverStitch Sx Endoscopic Suturing System | OCW | 2021-03-02 | View |
| 510(k) | K201808 | X-Tack Endoscopic HeliX Tacking System | PKL | 2020-12-15 | View |
| 510(k) | K171886 | OverStitch SX Endoscopic Suturing System (ESS) | OCW | 2017-11-15 | View |
No matching devices.