The following data is part of a premarket notification filed by Arthrex Inc. with the FDA for Arthrex Nanoscope System.
| Device ID | K190645 |
| 510k Number | K190645 |
| Device Name: | Arthrex NanoScope System |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | Arthrex Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Contact | Heli F. Chambi Infantas |
| Correspondent | Heli F. Chambi Infantas Arthrex Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-03-13 |
| Decision Date | 2019-07-05 |