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LORENZ ULTRA-MICRO TITANIUM OSTEOSYNTHESIS SYSTEM

K910038 Class II Traditional
Decision Date
1991-02-20
Sponsor / Applicant
Walter Lorenz Surgical, Inc.

Technical Specification

510(k) Submission ID K910038
Product Code JEY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4760
Decision Date 1991-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LORENZ ULTRA-MICRO TITANIUM OSTEOSYNTHESIS SYSTEM received FDA 510(k) clearance under submission number K910038, sponsored by Walter Lorenz Surgical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-02-20.

Classification & Regulation

This clearance is catalogued under FDA product code JEY and 21 CFR 872.4760, within the Dental review panel as a Class II device.