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XIA SPINE SYSTEM SACRAL BLOCK ASSEMBLY

K001653 Class II Traditional
Decision Date
2000-08-18
Sponsor / Applicant
Howmedica Osteonics Corp.

Technical Specification

510(k) Submission ID K001653
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2000-08-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XIA SPINE SYSTEM SACRAL BLOCK ASSEMBLY received FDA 510(k) clearance under submission number K001653, sponsored by Howmedica Osteonics 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 2000-08-18.

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.