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OSTEONICS TIBIAL TRAY SCREW HOLE PLUGS

K970779 Class II Traditional
Decision Date
1997-05-09
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K970779
Product Code LZN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 1997-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS TIBIAL TRAY SCREW HOLE PLUGS received FDA 510(k) clearance under submission number K970779, 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 1997-05-09.

Classification & Regulation

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