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ENCORE ANTERIOR SPINAL STAPLE SYSTEM

K030667 Class II Traditional
Decision Date
2003-05-28
Sponsor / Applicant
Encore Medical L.P.

Technical Specification

510(k) Submission ID K030667
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2003-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENCORE ANTERIOR SPINAL STAPLE SYSTEM received FDA 510(k) clearance under submission number K030667, sponsored by Encore Medical L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2003-05-28.

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.