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Hedgehog Cervical Interbody Fusion Device

Page Type
Cleared 510(K)
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)
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