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

Cervical Spinal Truss System (CSTS) Interbody Fusion Device

K Number: K173159 · Decision Jan 8, 2018
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
13
Review Days
101

Basic Information

Device Name
Cervical Spinal Truss System (CSTS) Interbody Fusion Device
K Number
K173159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
4Web, Inc.
Date Received
September 29, 2017
Decision Date
January 8, 2018
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

Similar 510(k) Clearances

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

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Other Clearances by 4Web, Inc.

K Number Device Name
K253201 Lumbar Spine Truss System - Plating Solution (LSTS-PS)
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)
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. →