meddevicedb.com FDA Device Reference

PROTRACT PRESS FIT HIP STEM-HA COATED

K010241 Class II Special
Decision Date
2001-02-08
Sponsor / Applicant
Stelkast Company

Technical Specification

510(k) Submission ID K010241
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2001-02-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTRACT PRESS FIT HIP STEM-HA COATED received FDA 510(k) clearance under submission number K010241, sponsored by Stelkast Company. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.