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TROCHANTER CABLE GRIP SYSTEM (ADD'L INDICATIONS)

K900926 Class II Traditional
Decision Date
1990-04-23
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K900926
Product Code LRN
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1990-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TROCHANTER CABLE GRIP SYSTEM (ADD'L INDICATIONS) received FDA 510(k) clearance under submission number K900926, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1990-04-23.

Classification & Regulation

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