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 |