Compass International CW-20
Compass International CW-20 is a Class II device made by Compass International, listed in FDA GUDID since 26 Aug 2016 (UDI-DI B169CW200), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB169CW200 | Date26 Aug 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Compass International
- Generic name
- Neurological stereotactic surgery system
- Model / Ref / Catalog
- CW-20
- Primary DI / UDI-DI
- B169CW200
- FDA product code
- HAW
- GMDN term
- Neurological stereotactic surgery system
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Neurological stereotactic surgery system.
- 20004 PercuNav Ultrasound Tracker 989605428083 by Philips Ultrasound LLC
- 10001 PercuNav Patient Tracker 989605427133 by Philips Ultrasound LLC
- Adapter for Flexsensor N 01 1949 by Fiagon GmbH
- EM Segment Tracker 9736512 by Medtronic Navigation Inc.
- StealthAiR 9734990 by Medtronic Navigation Inc.
- RADIOLUCENT DRAPELINK INTERCONNECTOR 19152-01 by Brainlab SE
- RADIOLUCENT DRAPELINK BASE SHORT 19153-04 by Brainlab SE
- SmartFrame NGS-XG-06 by Clearpoint Neuro, Inc.
- Navigation Headrest Universal E 01 1003 by Fiagon GmbH
- Leksell Vantage Stereotactic System 1040015 1040031 by Elekta Solutions AB