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510(k) clearance

Arthrex Spine Compression FT Screw

FDA 510(k) source

510(k) number
K262618
Applicant
Arthrex, Inc.
Decision date
Sep 24, 2026
Date received
Jul 28, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
MRW
Device type
System, Facet Screw Spinal Device
Device class
Unclassified
Advisory committee
Unknown
Statement or summary
Summary
Third party
N
Location
Naples, FL, US