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AugMENTA Penile Implant

Page Type
Cleared 510(K)
510(k) Number
K200073
510(k) Type
Traditional
Applicant
Augmenta LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2022
Days to Decision
990 days
Submission Type
Summary

AugMENTA Penile Implant

Page Type
Cleared 510(K)
510(k) Number
K200073
510(k) Type
Traditional
Applicant
Augmenta LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2022
Days to Decision
990 days
Submission Type
Summary