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SONGER CABLE SYSTEM

K922952 Class II Traditional
Decision Date
1993-02-23
Sponsor / Applicant
Pioneer Surgical Technology

Technical Specification

510(k) Submission ID K922952
Product Code JDQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3010
Decision Date 1993-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONGER CABLE SYSTEM received FDA 510(k) clearance under submission number K922952, sponsored by Pioneer Surgical Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1993-02-23.

Classification & Regulation

This clearance is catalogued under FDA product code JDQ and 21 CFR 888.3010, within the Orthopedic review panel as a Class II device.