meddevicedb.com FDA Device Reference

OSTEOMARK NTX POINT OF CARE (POC) CONTROL SET

K991917 Class I Traditional
Decision Date
1999-07-12
Sponsor / Applicant
Metrika, Inc.

Technical Specification

510(k) Submission ID K991917
Product Code JJW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1999-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEOMARK NTX POINT OF CARE (POC) CONTROL SET received FDA 510(k) clearance under submission number K991917, sponsored by Metrika, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1999-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code JJW and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.