meddevicedb.com FDA Device Reference

HANSEN-STREET TYPE INTRAMEDULLARY NAIL

K903256 Class II Traditional
Decision Date
1990-07-30
Sponsor / Applicant
Onyx Medical Corp.

Technical Specification

510(k) Submission ID K903256
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 1990-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HANSEN-STREET TYPE INTRAMEDULLARY NAIL received FDA 510(k) clearance under submission number K903256, sponsored by Onyx Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1990-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.