ARTAS System
FDA 510(k) clearance K173358 · decided 2018-03-16
Clearance details
- K-number
- K173358
- Device name
- ARTAS System
- Applicant
- Restoration Robotics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2017-10-25
- Decision date
- 2018-03-16
- Days to decision
- 142 days
- Clearance type
- Traditional
- Product code
- ONA
- Device class
- 2
- Regulation number
- 882.4560
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- San Josev, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| THE ARTAS SYSTEM (K123548) | Restoration Robotics, Inc. | 2013-02-25 |
| ARTAS SYSTEM FROM RESTORATION ROBOTICS (K123154) | Restoration Robotics, Inc. | 2013-02-19 |
| THE ARTAS SYSTEM FROM RESTORATION ROBOTICS (K103428) | Restoration Robotics, Inc. | 2011-04-04 |
Recalls involving this device
No recalls on record reference this clearance.