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Lateral Spinal Truss System (LSTS) Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K172392
510(k) Type
Traditional
Applicant
4Web, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2017
Days to Decision
91 days
Submission Type
Summary

Lateral Spinal Truss System (LSTS) Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K172392
510(k) Type
Traditional
Applicant
4Web, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2017
Days to Decision
91 days
Submission Type
Summary