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ABC CERVICAL PLATING SYSTEM

K000486 Class II Traditional
Decision Date
2000-04-14
Sponsor / Applicant
Aesculap, Inc.

Technical Specification

510(k) Submission ID K000486
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2000-04-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABC CERVICAL PLATING SYSTEM received FDA 510(k) clearance under submission number K000486, sponsored by Aesculap, 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 2000-04-14.

Classification & Regulation

This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.