The following data is part of a premarket notification filed by Field Orthopaedics Pty. Ltd. with the FDA for Field Orthopaedics Micro Screw System.
Device ID | K180348 |
510k Number | K180348 |
Device Name: | Field Orthopaedics Micro Screw System |
Classification | Screw, Fixation, Bone |
Applicant | Field Orthopaedics Pty. Ltd. 375 Wickham Terrace Brisbane, AU 4000 |
Contact | Christopher Jeffery |
Correspondent | Robert A Poggie BioVera Inc. 65 Promenade Saint Louis Notre-dame-del-l'ile-perrot, CA J7v 7p2 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-02-08 |
Decision Date | 2018-07-17 |
Summary: | summary |