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MICRO DYNAMIC MESH

K983528 Class II Traditional
Decision Date
1998-12-23
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K983528
Product Code JEY
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4760
Decision Date 1998-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO DYNAMIC MESH received FDA 510(k) clearance under submission number K983528, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1998-12-23.

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.