The following data is part of a premarket notification filed by Orthomet, Inc. with the FDA for Orthomet Orthopedic Staples.
| Device ID | K874914 |
| 510k Number | K874914 |
| Device Name: | ORTHOMET ORTHOPEDIC STAPLES |
| Classification | Staple, Fixation, Bone |
| Applicant | ORTHOMET, INC. 6301 CECILIA CIRCLE Minneapolis, MN 55439 -2713 |
| Contact | Al Lippincott |
| Correspondent | Al Lippincott ORTHOMET, INC. 6301 CECILIA CIRCLE Minneapolis, MN 55439 -2713 |
| Product Code | JDR |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-12-03 |
| Decision Date | 1988-02-04 |