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STRAIGHT-IN BONE SCREW FIXATION SYSTEM

K972622 Class II Traditional
Decision Date
1997-10-09
Sponsor / Applicant
Influence, Inc.

Technical Specification

510(k) Submission ID K972622
Product Code MBI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 1997-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRAIGHT-IN BONE SCREW FIXATION SYSTEM received FDA 510(k) clearance under submission number K972622, sponsored by Influence, 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 1997-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.