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 |