Ats Simulus Semi-Rigid Mitral Annuloplasty Ring, Model 800SC

FDA 510(k) K083683 · Genesee Biomedical, Inc.

Substantially Equivalent

510(k) numberK083683

Submission

Device name
Ats Simulus Semi-Rigid Mitral Annuloplasty Ring, Model 800SC
Applicant
Genesee Biomedical, Inc.
Denver, CO, US
Received
December 12, 2008
Decision date
February 25, 2009
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KRH – Ring, Annuloplasty
Device class
Class II (moderate risk)
Regulation
21 CFR 870.3800
Specialty
Cardiovascular
Implant
Yes

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K260498TriMemo™ SEMIRIGID ANNULOPLASTY RINGKRH · Abbreviated Corcym S.r.l.04/14/2026SE
K253232Seguin Annuloplasty RingKRH · Special Abbott Medical10/29/2025SE
K251982Edwards MC3 Tricuspid annuloplasty ring (4900)KRH · Abbreviated Edwards Lifesciences, LLC09/23/2025SE
K251688Carpentier-Edwards Physio Annuloplasty Ring (4450)KRH · Abbreviated Edwards Lifesciences, LLC09/17/2025SE
K250859TransForm McCarthy Mitral Annuloplasty Ring (TF)KRH · Traditional Genesee Biomedical, Inc.07/25/2025SE
K232599TransForm McCarthy Mitral Annuloplasty Ring (TF)KRH · Traditional Genesee Biomedical, Inc.04/09/2024SE
K230679WellsForm Tricuspid Annuloplasty Band (WF)KRH · Traditional Genesee Biomedical, Inc.05/26/2023SE
K230318Memo 3D Semirigid Annuloplasty Ring; Memo 3D ReChord Semirigid Annuloplasty Ring; Memo…KRH · Traditional Corcym S.r.l.04/07/2023SE
K202253TruForm Sievers Annuloplasty RingKRH · Traditional Genesee Biomedical, Inc.10/06/2020SE

More from Genesee Biomedical, Inc.

510(k)DeviceDecision
K252917ATLAAS (Atraumatic Left Atrial Appendage System) (AD)PZX · Traditional 05/22/2026SE
K250859TransForm McCarthy Mitral Annuloplasty Ring (TF)KRH · Traditional 07/25/2025SE
K232599TransForm McCarthy Mitral Annuloplasty Ring (TF)KRH · Traditional 04/09/2024SE
K230679WellsForm Tricuspid Annuloplasty Band (WF)KRH · Traditional 05/26/2023SE
K202253TruForm Sievers Annuloplasty RingKRH · Traditional 10/06/2020SE
K190506NeoForm Annuloplasty RingKRH · Traditional 04/18/2019SE
K161815FlexForm Annuloplasty Ring and FlexForm Annuloplasty BandKRH · Traditional 10/12/2016SE
K093903Ats Tri-Ad Semi-Flexible Tricuspid Anuuloplasty, Model 900SFCKRH · Special 07/15/2010SE
K090428Ats Simulus Adjustable Flexible Annuloplasty, Model 735 AcKRH · Special 05/07/2009SE
K072655Ats Simulus Semi-Rigid Mitral Annuloplasty Ring, Model 800SRKRH · Special 10/23/2007SE

Questions and answers

When was Ats Simulus Semi-Rigid Mitral Annuloplasty Ring, Model 800SC cleared by the FDA?

Ats Simulus Semi-Rigid Mitral Annuloplasty Ring, Model 800SC (K083683) received a 510(k) decision of Substantially Equivalent on February 25, 2009, 75 days after the submission was received.

What is the product code of K083683?

The FDA product code is KRH – Ring, Annuloplasty, a Class II (moderate risk) device regulated under 21 CFR 870.3800.