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Spectrum Spine Expandable Cages (SSEC)

K173518 Class II Traditional
Decision Date
2019-03-07
Sponsor / Applicant
Spectrum Spine, LLC

Technical Specification

510(k) Submission ID K173518
Product Code MAX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2019-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Spectrum Spine Expandable Cages (SSEC) received FDA 510(k) clearance under submission number K173518, sponsored by Spectrum Spine, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2019-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.