The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Quikplus System.
| Device ID | K970168 |
| 510k Number | K970168 |
| Device Name: | 3M QUIKPLUS SYSTEM |
| Classification | Crown And Bridge, Temporary, Resin |
| Applicant | 3M COMPANY 3M CENTER BLDG. 275-3SE-08 St. Paul, MN 55144 -1000 |
| Contact | Any Fowler |
| Correspondent | Any Fowler 3M COMPANY 3M CENTER BLDG. 275-3SE-08 St. Paul, MN 55144 -1000 |
| Product Code | EBG |
| CFR Regulation Number | 872.3770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-01-16 |
| Decision Date | 1997-02-27 |