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ADI 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
K191812
510(k) Type
Traditional
Applicant
Additive Device, Inc. (ADI) d/b/a restor3d
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2019
Days to Decision
111 days
Submission Type
Summary

ADI 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
K191812
510(k) Type
Traditional
Applicant
Additive Device, Inc. (ADI) d/b/a restor3d
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2019
Days to Decision
111 days
Submission Type
Summary