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LTM-T SURGICAL MESH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080353
510(k) Type
Traditional
Applicant
Lifecell Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2008
Days to Decision
52 days
Submission Type
Summary

LTM-T SURGICAL MESH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080353
510(k) Type
Traditional
Applicant
Lifecell Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2008
Days to Decision
52 days
Submission Type
Summary