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 |