The following data is part of a premarket notification filed by Wright Medical with the FDA for Dart-fire Edge Cannulated Screw System.
Device ID | K203228 |
510k Number | K203228 |
Device Name: | DART-FIRE EDGE Cannulated Screw System |
Classification | Screw, Fixation, Bone |
Applicant | Wright Medical 1023 Cherry Road Memphis, TN 38117 |
Contact | Michael Mullins |
Correspondent | Michael Mullins Wright Medical 1023 Cherry Road Memphis, TN 38117 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-11-02 |
Decision Date | 2021-05-11 |