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MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM

K032282 Class II Special
Decision Date
2003-08-21
Sponsor / Applicant
Implex Corp.

Technical Specification

510(k) Submission ID K032282
Product Code EZX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2003-08-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM received FDA 510(k) clearance under submission number K032282, sponsored by Implex Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-08-21.

Classification & Regulation

This clearance is catalogued under FDA product code EZX and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.