meddevicedb.com FDA Device Reference

HIP PIN

K813340 Class II Traditional
Decision Date
1982-01-29
Sponsor / Applicant
The Deca Co.

Technical Specification

510(k) Submission ID K813340
Product Code KTW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1982-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIP PIN received FDA 510(k) clearance under submission number K813340, sponsored by The Deca Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1982-01-29.

Classification & Regulation

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