The following data is part of a premarket notification filed by Osstem Implant Co Ltd with the FDA for Super Orthodontic Screw.
| Device ID | K062156 |
| 510k Number | K062156 |
| Device Name: | SUPER ORTHODONTIC SCREW |
| Classification | Implant, Endosseous, Root-form |
| Applicant | OSSTEM IMPLANT CO LTD 5536 TROWBRIDGE DRIVE Dunwoody, GA 30338 |
| Contact | Cathryn Cambria |
| Correspondent | Cathryn Cambria OSSTEM IMPLANT CO LTD 5536 TROWBRIDGE DRIVE Dunwoody, GA 30338 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-07-28 |
| Decision Date | 2006-10-20 |
| Summary: | summary |