Cleared Traditional

K102815 - SURELIFT PROLAPSE SYSTEM

K102815 is an FDA 510(k) clearance for SURELIFT PROLAPSE SYSTEM, manufactured by Neomedic International. The device is a Class 3 Obstetrics & Gynecology device with product code OTP cleared through the Traditional 510(k) pathway after a 282-day FDA review.

K102815 · Neomedic International · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2011
Decision
282d
Days
Class 3
Risk

K102815 is an FDA 510(k) clearance for the SURELIFT PROLAPSE SYSTEM. Classified as Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed (product code OTP), Class III - Premarket Approval.

Submitted by Neomedic International (Minneapolis, US). The FDA issued a Cleared decision on July 7, 2011 after a review of 282 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5980 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Neomedic International devices

FDA 510(k) Submission Details - K102815

510(k) Number K102815 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 28, 2010
Decision Date July 07, 2011
Days to Decision 282 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
122d slower than avg
Panel avg: 160d · This submission: 282d
Pathway characteristics
Predicate-based equivalence.

OTP Device Classification - Class 3, Premarket Approval

Product Code OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 884.5980
Definition Tissue Reinforcement Of The Fibromuscular Layer Of The Pelvic Floor When Surgical Treatment Is Indicated; Procedures Include Anterior And Posterior Vaginal Wall Prolapse Repair And Vaginal Apical Or Uterine Prolapse Repair Performed Transvaginally
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed

All 25
Devices cleared under the same product code (OTP) and FDA review panel - the closest regulatory comparables to K102815.
AMS ELEVATE PC
K112842 · American Medical Systems, Inc. · Oct 2011
LITE PELVIC FLOOR REPAIR KITS
K103426 · Boston Scientific Corp · Sep 2011
EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEM
K112386 · Coloplast Corp. · Sep 2011
EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEMS
K083499 · Coloplast A/S · May 2009
PELVIC FLOOR REPAIR SYSTEM
K091131 · Boston Scientific · May 2009
ELEVATE PROLAPSE REPAIR SYSTEM WITH PC COATED INTEPRO LITE- APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM, ANTERIOR AND AP
K090713 · American Medical Systems, Inc. · Apr 2009