Cleared Special

K014037 - SJM SEGUIN ANNULOPLASTY RING (SEGUIN RING), MODEL SARP-(SIZE)

K014037 is an FDA 510(k) clearance for SJM SEGUIN ANNULOPLASTY RING (SEGUIN RING), manufactured by St. Jude Medical, Inc.. The device is a Class 2 Cardiovascular device with product code KRH cleared through the Special 510(k) pathway after a 28-day FDA review.

K014037 · St. Jude Medical, Inc. · Cardiovascular device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jan 2002
Decision
28d
Days
Class 2
Risk

K014037 is an FDA 510(k) clearance for the SJM SEGUIN ANNULOPLASTY RING (SEGUIN RING), MODEL SARP-(SIZE). Classified as Ring, Annuloplasty (product code KRH), Class II - Special Controls.

Submitted by St. Jude Medical, Inc. (St. Paul, US). The FDA issued a Cleared decision on January 4, 2002 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3800 - the FDA cardiovascular device oversight 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.

FDA 510(k) Submission Details - K014037

510(k) Number K014037 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 2001
Decision Date January 04, 2002
Days to Decision 28 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
97d faster than avg
Panel avg: 125d · This submission: 28d
Pathway characteristics
Modification to existing cleared device.

KRH Device Classification - Class 2, Special Controls

Product Code KRH Ring, Annuloplasty
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.3800
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - KRH Ring, Annuloplasty

All 69
Devices cleared under the same product code (KRH) and FDA review panel - the closest regulatory comparables to K014037.
ANNULOFLO SYSTEM, MITRAL MODEL AR700
K021051 · Sulzer Carbomedics, Inc. · Apr 2002
EDWARDS MC TRICUSPID ANNULOPLASTY SYSTEM, MODEL 4900
K020864 · Edwards Lifesciences, LLC · Apr 2002
SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE)
K014161 · St. Jude Medical, Inc. · Jan 2002
MEDTRONIC COLVIN-GALLOWAY FUTURE ANNULOPLASTY BAND, MODEL 638B
K011395 · Medtronic Vascular · Jul 2001
SJM TAILOR ANNULOPLASTY RING, MODEL TARN
K000119 · St. Jude Medical, Inc. · Feb 2000
ANNULOFLEX ANNULOPLASTY SYSTEM, MODEL AF800
K992056 · Sulzer Carbomedics, Inc. · Oct 1999