meddevicedb.com FDA Device Reference

TOTAL KNEE SURGETICS NAVIGATION SYSTEM WITH IBLOCK

K090953 Class II Special
Decision Date
2010-01-21
Sponsor / Applicant
Praxim Medivision, SA

Technical Specification

510(k) Submission ID K090953
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2010-01-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL KNEE SURGETICS NAVIGATION SYSTEM WITH IBLOCK received FDA 510(k) clearance under submission number K090953, sponsored by Praxim Medivision, SA. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2010-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.