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ATRIUM PROLITE ULTRA S MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070192
510(k) Type
Special
Applicant
ATRIUM MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2007
Days to Decision
45 days
Submission Type
Statement

ATRIUM PROLITE ULTRA S MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070192
510(k) Type
Special
Applicant
ATRIUM MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2007
Days to Decision
45 days
Submission Type
Statement