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ATRIUM CENTRILFX MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110110
510(k) Type
Special
Applicant
ATRIUM MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2011
Days to Decision
32 days
Submission Type
Statement

ATRIUM CENTRILFX MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110110
510(k) Type
Special
Applicant
ATRIUM MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2011
Days to Decision
32 days
Submission Type
Statement