510(k) K221874

Altis Single Incision Sling System by Coloplast A/S — Product Code PAH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 15, 2023
Date Received
June 28, 2022
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling
Device Class
Class II
Regulation Number
878.3300
Review Panel
GU
Submission Type

Transvaginal surgical repair of female stress urinary incontinence (SUI) due to intrinsic sphincter deficiency (ISD) and/or urethral hypermobility.