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ATRIUM CENTRILFX MESH

Page Type
Cleared 510(K)
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)
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