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VerteFIT Corpectomy Cage System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162133
510(k) Type
Traditional
Applicant
Ldr Spine USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2017
Days to Decision
288 days
Submission Type
Summary

VerteFIT Corpectomy Cage System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162133
510(k) Type
Traditional
Applicant
Ldr Spine USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2017
Days to Decision
288 days
Submission Type
Summary