The following data is part of a premarket notification filed by Attachments Intl., Inc. with the FDA for Endosseous Implants.
| Device ID | K904236 |
| 510k Number | K904236 |
| Device Name: | ENDOSSEOUS IMPLANTS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | ATTACHMENTS INTL., INC. 600 S. AMPHLETT BLVD. San Mateo, CA 94402 |
| Contact | Peter Staubli |
| Correspondent | Peter Staubli ATTACHMENTS INTL., INC. 600 S. AMPHLETT BLVD. San Mateo, CA 94402 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-09-17 |
| Decision Date | 1991-11-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10841307122456 | K904236 | 000 |
| 10841307118268 | K904236 | 000 |
| 10841307118251 | K904236 | 000 |
| 10841307118244 | K904236 | 000 |
| 10841307118237 | K904236 | 000 |
| 10841307118015 | K904236 | 000 |
| 10841307118008 | K904236 | 000 |
| 10841307117995 | K904236 | 000 |
| 10841307117964 | K904236 | 000 |
| 10841307117940 | K904236 | 000 |
| 10841307117926 | K904236 | 000 |
| 10841307117919 | K904236 | 000 |
| 10841307117902 | K904236 | 000 |
| 10841307118299 | K904236 | 000 |
| 10841307118305 | K904236 | 000 |
| 10841307122449 | K904236 | 000 |
| 10841307122432 | K904236 | 000 |
| 10841307122401 | K904236 | 000 |
| 10841307122395 | K904236 | 000 |
| 10841307122388 | K904236 | 000 |
| 10841307122371 | K904236 | 000 |
| 10841307118640 | K904236 | 000 |
| 10841307118633 | K904236 | 000 |
| 10841307118565 | K904236 | 000 |
| 10841307118558 | K904236 | 000 |
| 10841307118527 | K904236 | 000 |
| 10841307118480 | K904236 | 000 |
| 10841307117896 | K904236 | 000 |