The following data is part of a premarket notification filed by Intuitive Surgical, Inc. with the FDA for Endowrist Mercury Bipolar Grasper.
Device ID | K180351 |
510k Number | K180351 |
Device Name: | EndoWrist Mercury Bipolar Grasper |
Classification | System, Surgical, Computer Controlled Instrument |
Applicant | Intuitive Surgical, Inc. 1266 Kifer Road Sunnyvale, CA 94086 |
Contact | Vishal Kanani |
Correspondent | Vishal Kanani Intuitive Surgical, Inc. 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 | 2018-02-08 |
Decision Date | 2018-08-07 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00886874115930 | K180351 | 000 |