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DUAL OFFSET PERFECTA IMC HIP STEM

K972641 Class II Traditional
Decision Date
1997-10-09
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K972641
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1997-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUAL OFFSET PERFECTA IMC HIP STEM received FDA 510(k) clearance under submission number K972641, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1997-10-09.

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.