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SELF-DRILLING RADIOGRAPHIC MARKER

K014148 Class II Special
Decision Date
2002-01-17
Sponsor / Applicant
Walter Lorenz Surgical, Inc.

Technical Specification

510(k) Submission ID K014148
Product Code NEU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2002-01-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SELF-DRILLING RADIOGRAPHIC MARKER received FDA 510(k) clearance under submission number K014148, sponsored by Walter Lorenz Surgical, Inc.. 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 2002-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code NEU and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.