The following data is part of a premarket notification filed by 3m Company with the FDA for Bone Stapling Fixation Sys.
| Device ID | K840566 |
| 510k Number | K840566 |
| Device Name: | BONE STAPLING FIXATION SYS |
| Classification | Staple, Fixation, Bone |
| Applicant | 3M COMPANY BUILDINGS 251-3 AND 270 St. Paul, MN 55144 -1000 |
| Contact | Willard D Larson |
| Correspondent | Willard D Larson 3M COMPANY BUILDINGS 251-3 AND 270 St. Paul, MN 55144 -1000 |
| Product Code | JDR |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-08 |
| Decision Date | 1984-11-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10845854031933 | K840566 | 000 |
| 20845854015671 | K840566 | 000 |
| 20845854015596 | K840566 | 000 |
| 20845854015589 | K840566 | 000 |
| 20845854015572 | K840566 | 000 |
| 10845854031735 | K840566 | 000 |
| 10845854031711 | K840566 | 000 |
| 10845854031759 | K840566 | 000 |
| 10845854031742 | K840566 | 000 |
| 20845854015688 | K840566 | 000 |
| 20845854015770 | K840566 | 000 |
| 10845854031766 | K840566 | 000 |
| 20845854016425 | K840566 | 000 |
| 20845854016296 | K840566 | 000 |
| 20845854016289 | K840566 | 000 |
| 20845854016067 | K840566 | 000 |
| 20845854016043 | K840566 | 000 |
| 20845854015923 | K840566 | 000 |
| 20845854015787 | K840566 | 000 |
| 10845854031728 | K840566 | 000 |