meddevicedb.com FDA Device Reference

Collagen Meniscus Implant XL

K170364 Class II Traditional
Decision Date
2017-05-02
Sponsor / Applicant
Ivy Sports Medicine, LLC

Technical Specification

510(k) Submission ID K170364
Product Code OLC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2017-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Collagen Meniscus Implant XL received FDA 510(k) clearance under submission number K170364, sponsored by Ivy Sports Medicine, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2017-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code OLC and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.