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Spectrum Spine, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253377Expandable Titanium PLIF/TLIF SystemOctober 24, 2025
K243074Spectrum Spine Lumbar Cage SystemApril 4, 2025
K240838Spectrum Spine Cervical Cage SystemMay 30, 2024
K201024Expandable Titanium PLIF/TLIF SystemApril 29, 2021
K173518Spectrum Spine Expandable Cages (SSEC)March 7, 2019
K132126SPECTRUM SPINE FENESTRATED FACET SCREW SYSTEMOctober 28, 2013
K122822SPECTRUM SPINE LAMINOPLASTY PLATING SYSTEMFebruary 7, 2013