The following data is part of a premarket notification filed by Intuitive Surgical, Inc. with the FDA for Da Vinci S/si Endoscopes, Da Vinci Xi Endoscopes.
| Device ID | K170641 |
| 510k Number | K170641 |
| Device Name: | Da Vinci S/Si Endoscopes, Da Vinci Xi Endoscopes |
| Classification | System, Surgical, Computer Controlled Instrument |
| Applicant | Intuitive Surgical, Inc. 1266 Kifer Road, Building 101 Sunnyvale, CA 94086 |
| Contact | Kunal Gunjal |
| Correspondent | Kunal Gunjal Intuitive Surgical, Inc. 1266 Kifer Road, Building 101 Sunnyvale, CA 94086 |
| Product Code | NAY |
| Subsequent Product Code | GCJ |
| Subsequent Product Code | IZI |
| Subsequent Product Code | OWN |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-02 |
| Decision Date | 2017-09-21 |
| Summary: | summary |