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GLOBAL PRESS-FIT STEM

K032385 Class II Traditional
Decision Date
2003-10-30
Sponsor / Applicant
Global Medical Co.

Technical Specification

510(k) Submission ID K032385
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2003-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLOBAL PRESS-FIT STEM received FDA 510(k) clearance under submission number K032385, sponsored by Global Medical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2003-10-30.

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.