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

Hammertoe Truss System (HTS)

K Number: K190926 · Decision Jul 23, 2019
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
13
Review Days
105

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Basic Information

Device Name
Hammertoe Truss System (HTS)
K Number
K190926
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
4Web, Inc.
Date Received
April 9, 2019
Decision Date
July 23, 2019
Product Code
HTY
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
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HTY), 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)
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. →