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INSTINCT JAVA SYSTEM

K123552 Class II Traditional
Decision Date
2013-04-19
Sponsor / Applicant
Zimmer Spine

Technical Specification

510(k) Submission ID K123552
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2013-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTINCT JAVA SYSTEM received FDA 510(k) clearance under submission number K123552, sponsored by Zimmer Spine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.