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 |