The following data is part of a premarket notification filed by Stick Tech Ltd. with the FDA for Everstick Post.
| Device ID | K030820 |
| 510k Number | K030820 |
| Device Name: | EVERSTICK POST |
| Classification | Post, Root Canal |
| Applicant | STICK TECH LTD. 80 PARKWAY WEST Mount Vernon, NY 10552 |
| Contact | William Troetel |
| Correspondent | William Troetel STICK TECH LTD. 80 PARKWAY WEST Mount Vernon, NY 10552 |
| Product Code | ELR |
| CFR Regulation Number | 872.3810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-03-14 |
| Decision Date | 2003-05-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| J0229008271 | K030820 | 000 |
| 15400556008673 | K030820 | 000 |
| 15400556008666 | K030820 | 000 |
| 15400556008659 | K030820 | 000 |