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DURA-GUARD-DURAL REPAIR PATCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973706
510(k) Type
Traditional
Applicant
BIO-VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/1997
Days to Decision
86 days
Submission Type
Summary

DURA-GUARD-DURAL REPAIR PATCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973706
510(k) Type
Traditional
Applicant
BIO-VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/1997
Days to Decision
86 days
Submission Type
Summary