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MILAGRO Interference Screw; MILAGRO ADVANCE Interference Screw

K240441 Class II Special
Decision Date
2024-03-15
Sponsor / Applicant
Depuy Mitek

Technical Specification

510(k) Submission ID K240441
Product Code MAI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2024-03-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILAGRO Interference Screw; MILAGRO ADVANCE Interference Screw received FDA 510(k) clearance under submission number K240441, sponsored by Depuy Mitek. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code MAI and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.