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Lateral Spinal Truss System (LSTS) Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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