meddevicedb.com FDA Device Reference

HOFFMANN II MIAMI POST

K983419 Class II Traditional
Decision Date
1998-11-25
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K983419
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1998-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOFFMANN II MIAMI POST received FDA 510(k) clearance under submission number K983419, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1998-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.