← Product Code [LML](/productcode/LML) · P850069S006

# KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069S006)

_3M Company · LML · Dec 31, 1992 · Orthopedic · APPR_

**Canonical URL:** https://fda.innolitics.com/device/P850069S006

## Device Facts

- **Applicant:** 3M Company
- **Product Code:** [LML](/productcode/LML.md)
- **Decision Date:** Dec 31, 1992
- **Decision:** APPR
- **Device Class:** Class 3
- **Review Panel:** Orthopedic

---

**Source:** [https://fda.innolitics.com/device/P850069S006](https://fda.innolitics.com/device/P850069S006)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a PMA](https://innolitics.com/services/regulatory/), [a 510(k)](https://innolitics.com/services/510ks/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
