CorPath GRX System
510(k) K202275
CorPath GRX System is a Class II device made by Corindus, Inc., cleared under FDA 510(k) K202275 on 11 Dec 2020, active as of 9 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK202275 | Date11 Dec 2020 | StatusActive |
Official records
- FDA 510(k) database K202275
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- DXX
- Device class
- Class II
- Regulation
- 21 CFR Part 870.1290
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K202275
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| CorPath GRX Cassette 305 | 305 / 305 | 00816280023055 | No longer on the market | |
| CorPath GRX Control Console 301 | 301 / 301 | 00816280023017 | No longer on the market | |
| CorPath GRX Drape, Control Console 311 | 311 / 311 | 00816280023116 | No longer on the market | |
| CorPath GRX Drape, Robotic Drive and Arm 309 | 309 / 309 | 00816280023093 | No longer on the market | |
| CorPath GRX Drive Gear 307 | 307 / 307 | 00816280023079 | No longer on the market | |
| CorPath GRX Extended Reach Arm 312 | 312 / 312 | 00816280023123 | No longer on the market |
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