Last synced on 14 November 2025 at 11:06 pm

ELEVATE PROLAPSE REPAIR SYSTEM WITH PC COATED INTEPRO LITE- APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM, ANTERIOR AND AP

Page Type
Cleared 510(K)
510(k) Number
K090713
510(k) Type
Special
Applicant
AMERICAN MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2009
Days to Decision
15 days
Submission Type
Summary

ELEVATE PROLAPSE REPAIR SYSTEM WITH PC COATED INTEPRO LITE- APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM, ANTERIOR AND AP

Page Type
Cleared 510(K)
510(k) Number
K090713
510(k) Type
Special
Applicant
AMERICAN MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2009
Days to Decision
15 days
Submission Type
Summary