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DURAGEN DURAL GRAFT MATRIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982180
510(k) Type
Traditional
Applicant
INTEGRA LIFESCIENCES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1999
Days to Decision
379 days
Submission Type
Summary

DURAGEN DURAL GRAFT MATRIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982180
510(k) Type
Traditional
Applicant
INTEGRA LIFESCIENCES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1999
Days to Decision
379 days
Submission Type
Summary