The following data is part of a premarket notification filed by Intuitive Surgical, Inc. with the FDA for Da Vinci X Surgical System.
Device ID | K171294 |
510k Number | K171294 |
Device Name: | Da Vinci X Surgical System |
Classification | System, Surgical, Computer Controlled Instrument |
Applicant | Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 |
Contact | Brandon Hansen |
Correspondent | Brandon Hansen Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 |
Product Code | NAY |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-02 |
Decision Date | 2017-05-26 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00886874115404 | K171294 | 000 |