# K182964 (us_fda)

FDA 510(k) clearance for the Zimmer Biomet ROSA Knee System; reported 2019.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K182964
- Filing date: 2018-10-25
- Decision date: 2019-01-24
- Verification posture: reported
- Cap-flag notes: Filing number not yet captured. Upgrade to verified when the K-number is confirmed.

## Applicant

- [Zimmer Biomet](/companies/zimmer-biomet.md)

## Covered models (1)

- [ROSA](/models/zimmer-biomet-rosa.md)

## Sources (1)

- [https://www.zimmerbiomet.com](https://www.zimmerbiomet.com)

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