# K242121 (us_fda)

FDA 510(k) clearance for the Monogram mBos / semi-autonomous total-knee-arthroplasty system; reported March 2025.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K242121
- Filing date: 2024-07-19
- Decision date: 2025-03-14
- Verification posture: reported
- Cap-flag notes: Filing number not yet captured; clearance reported March 2025. Upgrade to verified when the K-number is confirmed.

## Applicant

- [Monogram Technologies](/companies/monogram.md)

## Covered models (1)

- [mBos TKA System](/models/monogram-mbos.md)

## Sources (1)

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

_Canonical URL: /regulatory-filings/fda-monogram-mbos-clearance-2025. HTML version: [/regulatory-filings/fda-monogram-mbos-clearance-2025](/regulatory-filings/fda-monogram-mbos-clearance-2025)._