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FOUNDATION POROUS STEM

K935263 Class II Traditional
Decision Date
1995-07-11
Sponsor / Applicant
Encore Orthopedics, Inc.

Technical Specification

510(k) Submission ID K935263
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1995-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FOUNDATION POROUS STEM received FDA 510(k) clearance under submission number K935263, sponsored by Encore Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1995-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.