The following data is part of a premarket notification filed by The Stern Metals Co., Inc. with the FDA for Endosseous Implants.
| Device ID | K924219 |
| 510k Number | K924219 |
| Device Name: | ENDOSSEOUS IMPLANTS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | THE STERN METALS CO., INC. 23 FRANK MOSSBERG DR. Attleboro, MA 02703 |
| Contact | Walton, Jr. |
| Correspondent | Walton, Jr. THE STERN METALS CO., INC. 23 FRANK MOSSBERG DR. Attleboro, MA 02703 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-21 |
| Decision Date | 1994-02-14 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08415491044990 | K924219 | 000 |
| 00841549106972 | K924219 | 000 |