FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Lumbar Spine Truss System - Plating Solution (LSTS-PS)

K Number: K253201 · Decision Feb 12, 2026
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
13
Review Days
139

Basic Information

Device Name
Lumbar Spine Truss System - Plating Solution (LSTS-PS)
K Number
K253201
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
4Web, Inc.
Date Received
September 26, 2025
Decision Date
February 12, 2026
Product Code
KWQ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWQ), ordered by most recent decision date.

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Other Clearances by 4Web, Inc.

K Number Device Name
K203065 Lumbar Spine Truss System Plating Solution (LSTS-PS)
K200002 Anterior Spine Truss System – Stand Alone (ASTS-SA) Interbody Fusion Device
K190870 Cervical Spinal Truss System-Stand Alone (CSTS-SA)
K190926 Hammertoe Truss System (HTS)
K172294 Osteotomy Truss System (OTS)
K173159 Cervical Spinal Truss System (CSTS) Interbody Fusion Device
K172392 Lateral Spinal Truss System (LSTS) Interbody Fusion Device
K171351 Posterior Spine Truss System (PSTS) Interbody Fusion Device
K170851 Anterior Spine Truss System (STS) Interbody Fusion Device
K153436 LATERAL Spine Truss System
Search all 13 clearances from 4Web, Inc. →