This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
| Device | P180008S004 | 
| Classification Name | None | 
| Applicant | |
| PMA | P180008 | 
| Supplement | S004 | 
| Supplement Number | Date | Supplement Type | 
|---|---|---|
| P180008 | Original Filing | |
| S007 | 2019-11-20 | 30-day Notice | 
| S006 | 2018-09-27 | 30-day Notice | 
| S005 | 2018-09-12 | 30-day Notice | 
| S004 | ||
| S003 | 2018-08-31 | Real-time Process | 
| S002 | 2018-08-31 | Real-time Process | 
| S001 | 2018-08-31 | Real-time Process | 
| Device ID | PMA | Supp | 
|---|---|---|
| 00853052007325 | P180008 | 000 | 
| 00853052007301 | P180008 | 000 | 
| 00853052007288 | P180008 | 000 | 
| 00853052007264 | P180008 | 000 | 
| 00850006613380 | P180008 | 000 | 
| 00850006613373 | P180008 | 000 |