The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Arthrex Mesh Plate System.
| Device ID | K170547 |
| 510k Number | K170547 |
| Device Name: | Arthrex Mesh Plate System |
| Classification | Plate, Fixation, Bone |
| Applicant | Arthrex, Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Contact | Ivette Galmez |
| Correspondent | Ivette Galmez Arthrex, Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-02-24 |
| Decision Date | 2017-09-01 |
| Summary: | summary |