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ADI TiDAL Osteotomy Wedge

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191047
510(k) Type
Traditional
Applicant
Additive Device, Inc. (Adi) D/B/A Restor3D
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2019
Days to Decision
200 days
Submission Type
Summary

ADI TiDAL Osteotomy Wedge

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191047
510(k) Type
Traditional
Applicant
Additive Device, Inc. (Adi) D/B/A Restor3D
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2019
Days to Decision
200 days
Submission Type
Summary