Last synced on 14 November 2025 at 11:06 pm

EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K083499
510(k) Type
Traditional
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
164 days
Submission Type
Summary

EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K083499
510(k) Type
Traditional
Applicant
COLOPLAST A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
164 days
Submission Type
Summary