Last synced on 6 December 2024 at 11:05 pm

LIFECELL DURAL SUBSTITUTE MATRIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061208
510(k) Type
Traditional
Applicant
LIFECELL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2007
Days to Decision
247 days
Submission Type
Summary

LIFECELL DURAL SUBSTITUTE MATRIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061208
510(k) Type
Traditional
Applicant
LIFECELL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2007
Days to Decision
247 days
Submission Type
Summary