The following data is part of a premarket notification filed by In2bones Usa, Llc with the FDA for Fracture And Correction System.
| Device ID | K180377 |
| 510k Number | K180377 |
| Device Name: | Fracture And Correction System |
| Classification | Screw, Fixation, Bone |
| Applicant | In2Bones USA, LLC 6060 Poplar Ave, Suite 380 Memphis, TN 38119 |
| Contact | Rebecca Wahl |
| Correspondent | Christine Scifert MRC-X, LLC 6075 Poplar Avenue, Suite 500 Memphis, TN 38119 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-02-12 |
| Decision Date | 2018-06-20 |
| Summary: | summary |