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EMERGE MEDICAL SOLID BONE SCREWS

K122489 Class II Traditional
Decision Date
2012-12-10
Sponsor / Applicant
Emerge Medical

Technical Specification

510(k) Submission ID K122489
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2012-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMERGE MEDICAL SOLID BONE SCREWS received FDA 510(k) clearance under submission number K122489, sponsored by Emerge Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-12-10.

Classification & Regulation

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