Last synced on 20 December 2024 at 11:05 pm

DURAFORM Dural Graft Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152481
510(k) Type
Special
Applicant
CODMAN & SHURTLEFF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2015
Days to Decision
60 days
Submission Type
Summary

DURAFORM Dural Graft Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152481
510(k) Type
Special
Applicant
CODMAN & SHURTLEFF, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2015
Days to Decision
60 days
Submission Type
Summary