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Hedgehog Cervical Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143685
510(k) Type
Traditional
Applicant
Vertera, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2015
Days to Decision
273 days
Submission Type
Summary

Hedgehog Cervical Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143685
510(k) Type
Traditional
Applicant
Vertera, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2015
Days to Decision
273 days
Submission Type
Summary