meddevicedb.com FDA Device Reference

POLY PLUG CEMENT RESTRICTOR

K840242 Class II Traditional
Decision Date
1984-05-30
Sponsor / Applicant
Latham Manufacturer

Technical Specification

510(k) Submission ID K840242
Product Code JDS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1984-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLY PLUG CEMENT RESTRICTOR received FDA 510(k) clearance under submission number K840242, sponsored by Latham Manufacturer. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1984-05-30.

Classification & Regulation

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