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APEX FIXATION PINS

K001886 Class II Special
Decision Date
2000-07-12
Sponsor / Applicant
Howmedica Osteonics Corp.

Technical Specification

510(k) Submission ID K001886
Product Code JDW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2000-07-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APEX FIXATION PINS received FDA 510(k) clearance under submission number K001886, sponsored by Howmedica Osteonics Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code JDW and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.