Cleared Special

K132054 - GYNECARE TVT EXACT CONTINENCE SYSTEM

K132054 is an FDA 510(k) clearance for GYNECARE TVT EXACT CONTINENCE SYSTEM, manufactured by Ethicon, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code OTN cleared through the Special 510(k) pathway after a 51-day FDA review.

K132054 · Ethicon, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2013
Decision
51d
Days
Class 2
Risk

K132054 is an FDA 510(k) clearance for the GYNECARE TVT EXACT CONTINENCE SYSTEM. Classified as Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator (product code OTN), Class II - Special Controls.

Submitted by Ethicon, Inc. (Somerville, US). The FDA issued a Cleared decision on August 23, 2013 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 878.3300 - the FDA gastroenterology and urology device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Ethicon, Inc. devices

FDA 510(k) Submission Details - K132054

510(k) Number K132054 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 03, 2013
Decision Date August 23, 2013
Days to Decision 51 days
Submission Type Special
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d faster than avg
Panel avg: 131d · This submission: 51d
Pathway characteristics
Modification to existing cleared device.

OTN Device Classification - Class 2, Special Controls

Product Code OTN Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.3300
Definition Surgical Treatment Of Female Stress Urinary Incontinence Due To Intrinsic Sphincter Deficiency (isd) And/or Urethral Hypermobility
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - OTN Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator

All 44
Devices cleared under the same product code (OTN) and FDA review panel - the closest regulatory comparables to K132054.
Desara TV, Desara Blue TV
K162201 · Caldera Medical, Inc. · Jan 2017
RETROARC RETROPUBIC SLING SYSTEM
K132655 · American Medical Systems, Inc. · Nov 2013
DESARA MESH, DESARA BLUE
K132069 · Caldera Medical, Inc. · Sep 2013
DESARA SL
K121928 · Caldera Medical, Inc. · Feb 2013
BLUE SUI SLING
K121754 · Boston Scientific Corp · Oct 2012
DESARA MESH
K112609 · Caldera Medical, Inc. · Sep 2011