510(k) K073646

MINITAPE URETHRAL SLING by Mpathy Medical Devices, Ltd. — Product Code PAH

K073646 is an FDA 510(k) premarket notification submitted by Mpathy Medical Devices, Ltd. for the device "MINITAPE URETHRAL SLING". The FDA issued a decision of Substantially Equivalent on February 25, 2008. The device falls under product code PAH (Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling), a Class II device regulated under 21 CFR 878.3300. Mpathy Medical Devices, Ltd. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 25, 2008
Date Received
December 26, 2007
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.