The following data is part of a premarket notification filed by Stick Tech Ltd. with the FDA for Everstick Perio.
| Device ID | K030072 |
| 510k Number | K030072 |
| Device Name: | EVERSTICK PERIO |
| Classification | Resin, Denture, Relining, Repairing, Rebasing |
| Applicant | STICK TECH LTD. 80 PARKWAY WEST Mount Vernon, NY 10552 |
| Contact | William M Troetel |
| Correspondent | William M Troetel STICK TECH LTD. 80 PARKWAY WEST Mount Vernon, NY 10552 |
| Product Code | EBI |
| CFR Regulation Number | 872.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-01-08 |
| Decision Date | 2003-04-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00842092112656 | K030072 | 000 |
| J0229008221 | K030072 | 000 |
| 15400556008697 | K030072 | 000 |
| 15400556008598 | K030072 | 000 |