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ANATOMICA POSTERIOR CERVICAL FIXATION SYSTEM

K061943 Class II Traditional
Decision Date
2007-05-25
Sponsor / Applicant
Anatomica AB

Technical Specification

510(k) Submission ID K061943
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2007-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANATOMICA POSTERIOR CERVICAL FIXATION SYSTEM received FDA 510(k) clearance under submission number K061943, sponsored by Anatomica AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-05-25.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.