FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MINITAPE EXTRA URETHRAL SLING

K Number: K073647 · Decision Mar 3, 2008
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
64
Applicant Total
6
Review Days
68

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Basic Information

Device Name
MINITAPE EXTRA URETHRAL SLING
K Number
K073647
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mpathy Medical Devices, Ltd.
Date Received
December 26, 2007
Decision Date
March 3, 2008
Product Code
OTN
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OTN Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OTN), ordered by most recent decision date.

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Other Clearances by Mpathy Medical Devices, Ltd.

K Number Device Name
K092203 OMNISURE URETHRAL SLING, MODEL OTK52
K091180 MINITAPE URETHRAL SLING
K073646 MINITAPE URETHRAL SLING
K053361 MODIFICATION TO: MINIMESH POLYPROPYLENE MESH
K041632 MINIMESH POLYPROPYLENE MESH