The following data is part of a premarket notification filed by Intuitive Surgical with the FDA for Da Vinci Xi Surgical System.
Device ID | K152892 |
510k Number | K152892 |
Device Name: | Da Vinci Xi Surgical System |
Classification | System, Surgical, Computer Controlled Instrument |
Applicant | INTUITIVE SURGICAL 1266 KIFER ROAD Sunnyvale, CA 94086 |
Contact | Crystal Ong |
Correspondent | Crystal Ong INTUITIVE SURGICAL 1266 KIFER ROAD Sunnyvale, CA 94086 |
Product Code | NAY |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-30 |
Decision Date | 2016-04-29 |
Summary: | summary |