The following data is part of a premarket notification filed by 3m Medical Products Group with the FDA for Precise Barnd Pi Disposable Surgical Staples.
| Device ID | K911252 |
| 510k Number | K911252 |
| Device Name: | PRECISE BARND PI DISPOSABLE SURGICAL STAPLES |
| Classification | Staple, Implantable |
| Applicant | 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul, MN 55144 -1000 |
| Contact | Carl M Story |
| Correspondent | Carl M Story 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul, MN 55144 -1000 |
| Product Code | GDW |
| CFR Regulation Number | 878.4750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-03-21 |
| Decision Date | 1991-07-25 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884521066899 | K911252 | 000 |
| 30884521066513 | K911252 | 000 |
| 20884521065106 | K911252 | 000 |
| 20884521065120 | K911252 | 000 |
| 20884521065137 | K911252 | 000 |
| 20884521065168 | K911252 | 000 |
| 20884521066462 | K911252 | 000 |
| 20884521066479 | K911252 | 000 |
| 20884521066486 | K911252 | 000 |
| 20884521066523 | K911252 | 000 |
| 20884521066530 | K911252 | 000 |
| 30884521066506 | K911252 | 000 |