meddevicedb.com FDA Device Reference

SURGICAL KNIVES & PROBES

K802479 Class I Traditional
Decision Date
1980-10-31
Sponsor / Applicant
Eder Instrument Co, Inc.

Technical Specification

510(k) Submission ID K802479
Product Code HXB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4540
Decision Date 1980-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL KNIVES & PROBES received FDA 510(k) clearance under submission number K802479, sponsored by Eder Instrument Co, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1980-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code HXB and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.