meddevicedb.com FDA Device Reference

Internal Joint Stabilizer - Elbow

K153208 Class II Traditional
Decision Date
2015-12-31
Sponsor / Applicant
Skeletal Dynamics, LLC

Technical Specification

510(k) Submission ID K153208
Product Code OZI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2015-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Internal Joint Stabilizer - Elbow received FDA 510(k) clearance under submission number K153208, sponsored by Skeletal Dynamics, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-12-31.

Classification & Regulation

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