# K171120 (us_fda)

Foundational US FDA 510(k) clearance of the Senhance Surgical Robotic System; filed by TransEnterix, Inc. (later renamed Asensus Surgical). (The earlier De Novo DEN160056 could not be corroborated to a primary record - honest-absence.)

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K171120
- Filing date: 2017-04-14
- Decision date: 2017-10-13
- Verification posture: verified

## Applicant

- [Asensus Surgical](/companies/asensus-surgical.md)

## Covered models (1)

- [Senhance](/models/asensus-senhance.md)

## Sources (1)

- [https://api.fda.gov/device/510k.json?search=k_number:K171120](https://api.fda.gov/device/510k.json?search=k_number:K171120)

_Canonical URL: /regulatory-filings/fda-510k-senhance-2017. HTML version: [/regulatory-filings/fda-510k-senhance-2017](/regulatory-filings/fda-510k-senhance-2017)._