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OSTEONICS MICROSTRUCTURED ACETABULAR COMPONENTS

K925883 Class II Traditional
Decision Date
1993-06-15
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K925883
Product Code JDJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 1993-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS MICROSTRUCTURED ACETABULAR COMPONENTS received FDA 510(k) clearance under submission number K925883, sponsored by Osteonics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1993-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code JDJ and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.