Last synced on 2 May 2025 at 11:05 pm

Collagen Dural Regeneration Matrix

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150825
510(k) Type
Traditional
Applicant
COLLAGEN MATRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2015
Days to Decision
238 days
Submission Type
Summary

Collagen Dural Regeneration Matrix

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150825
510(k) Type
Traditional
Applicant
COLLAGEN MATRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2015
Days to Decision
238 days
Submission Type
Summary