meddevicedb.com FDA Device Reference

Shoulder Soft Tissue Anchors

K242477 Class II Traditional
Decision Date
2025-05-12
Sponsor / Applicant
Signature Orthopaedics Pty, Ltd.

Technical Specification

510(k) Submission ID K242477
Product Code MBI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2025-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Shoulder Soft Tissue Anchors received FDA 510(k) clearance under submission number K242477, sponsored by Signature Orthopaedics Pty, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.