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AMS ELEVATE PC APICAL AND POSTERIOR ( AND ANTERIOR AND APICAL) PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111118
510(k) Type
Special
Applicant
AMERICAN MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2011
Days to Decision
71 days
Submission Type
Summary

AMS ELEVATE PC APICAL AND POSTERIOR ( AND ANTERIOR AND APICAL) PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111118
510(k) Type
Special
Applicant
AMERICAN MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2011
Days to Decision
71 days
Submission Type
Summary