meddevicedb.com FDA Device Reference

A/K SOCKET

K802911 Class I Traditional
Decision Date
1980-12-17
Sponsor / Applicant
Orthomedics

Technical Specification

510(k) Submission ID K802911
Product Code ISS
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3420
Decision Date 1980-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A/K SOCKET received FDA 510(k) clearance under submission number K802911, sponsored by Orthomedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1980-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code ISS and 21 CFR 890.3420, within the Physical Medicine review panel as a Class I device.