The following data is part of a premarket notification filed by Intuitive Surgical, Inc. with the FDA for Intuitive Surgical Da Vinci Surgical System, Model Is2000.
Device ID | K050369 |
510k Number | K050369 |
Device Name: | INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODEL IS2000 |
Classification | System, Surgical, Computer Controlled Instrument |
Applicant | INTUITIVE SURGICAL, INC. 950 KIFER RD. Sunnyvale, CA 94086 -5206 |
Contact | Michael H Yramategui |
Correspondent | Michael H Yramategui INTUITIVE SURGICAL, INC. 950 KIFER RD. Sunnyvale, CA 94086 -5206 |
Product Code | NAY |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-02-14 |
Decision Date | 2005-04-29 |
Summary: | summary |