4Web, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
2
Compliance Actions
0

Known Names

4web, 4-web

Recent 510(k) Clearances

K-NumberDeviceDate
K253201Lumbar Spine Truss System - Plating Solution (LSTS-PS)February 12, 2026
K203065Lumbar Spine Truss System Plating Solution (LSTS-PS)March 10, 2021
K200002Anterior Spine Truss System – Stand Alone (ASTS-SA) Interbody Fusion DeviceMay 29, 2020
K190870Cervical Spinal Truss System-Stand Alone (CSTS-SA)August 12, 2019
K190926Hammertoe Truss System (HTS)July 23, 2019
K172294Osteotomy Truss System (OTS)February 22, 2018
K173159Cervical Spinal Truss System (CSTS) Interbody Fusion DeviceJanuary 8, 2018
K172392Lateral Spinal Truss System (LSTS) Interbody Fusion DeviceNovember 7, 2017
K171351Posterior Spine Truss System (PSTS) Interbody Fusion DeviceSeptember 8, 2017
K170851Anterior Spine Truss System (STS) Interbody Fusion DeviceAugust 7, 2017
K153436LATERAL Spine Truss SystemJune 6, 2016
K143258PLIF STS, TLIF STS, OLIF STS (Spinal Truss System)April 9, 2015
K1421124WEB SPINAL IMPLANT PRODUCTSSeptember 23, 2014