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LigaPASS™ 2.0 Ligament Augmentation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213659
510(k) Type
Traditional
Applicant
Medicrea International S. A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/24/2022
Days to Decision
186 days
Submission Type
Summary

LigaPASS™ 2.0 Ligament Augmentation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213659
510(k) Type
Traditional
Applicant
Medicrea International S. A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/24/2022
Days to Decision
186 days
Submission Type
Summary