meddevicedb.com FDA Device Reference

DIGIT-GRIP WITH LCD (DGR002)

K970870 Class I Traditional
Decision Date
1997-05-02
Sponsor / Applicant
Nk Biotechnical Corp.

Technical Specification

510(k) Submission ID K970870
Product Code HRW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1250
Decision Date 1997-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGIT-GRIP WITH LCD (DGR002) received FDA 510(k) clearance under submission number K970870, sponsored by Nk Biotechnical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1997-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code HRW and 21 CFR 888.1250, within the Orthopedic review panel as a Class I device.