meddevicedb.com FDA Device Reference

HIP FRACTURE STEM SYSTEM - FENESTRATION PLUG

K890326 Class II Traditional
Decision Date
1989-02-03
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K890326
Product Code LZN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 1989-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIP FRACTURE STEM SYSTEM - FENESTRATION PLUG received FDA 510(k) clearance under submission number K890326, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1989-02-03.

Classification & Regulation

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