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THE TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 10-340-XXXXX

K040756 Class II Special
Decision Date
2004-07-14
Sponsor / Applicant
Implex Corp.

Technical Specification

510(k) Submission ID K040756
Product Code FTM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2004-07-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 10-340-XXXXX received FDA 510(k) clearance under submission number K040756, 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 2004-07-14.

Classification & Regulation

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