Triton® 720202
by Medtronic Powered Surgical Solutions
Triton® 720202 is a Class I device made by Medtronic Powered Surgical Solutions, cleared under FDA 510(k) K870157 on 24 Feb 1987 and listed in FDA GUDID since 29 Apr 2016 (UDI-DI 00613994444523), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00613994444523 | Date29 Apr 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK870157 | Date24 Feb 1987 | StatusActive |
Official records
- AccessGUDID record 00613994444523
- FDA 510(k) database K870157
Across registries
- FDA 510(k) K870157 decided 24 Feb 1987 Active
- FDA GUDID UDI-DI 00613994444523 listed 29 Apr 2016 Listed
Timeline
- Cleared FDA 510(k) K870157
- Listed FDA GUDID 00613994444523
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Triton®
- Generic name
- Surgical power tool system control unit, pneumatic
- Model / reference
- 720202
- Primary DI / UDI-DI
- 00613994444523
- 510(k) Number
- FDA product code
- KFK
- GMDN term
- Surgical power tool system control unit, pneumatic
- Device class
- Class I
- Regulation number
- 878.4820
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Surgical power tool system control unit, pneumatic.