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ATRIUM LITE MESH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002093
510(k) Type
Special
Applicant
Atrium Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2000
Days to Decision
13 days
Submission Type
Statement

ATRIUM LITE MESH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002093
510(k) Type
Special
Applicant
Atrium Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2000
Days to Decision
13 days
Submission Type
Statement