The following data is part of a premarket notification filed by Tornier, Inc. with the FDA for Forefoot Stp System.
| Device ID | K150871 |
| 510k Number | K150871 |
| Device Name: | ForeFoot STP System |
| Classification | Screw, Fixation, Bone |
| Applicant | TORNIER, INC. 1065 MEDINA RD, SUITE 500 Medina, OH 44256 |
| Contact | Brian Hockett |
| Correspondent | Brian Hockett TORNIER, INC. 1065 MEDINA RD, SUITE 500 Medina, OH 44256 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-04-01 |
| Decision Date | 2015-08-04 |
| Summary: | summary |