Ats Simulus Annuloplasty Band, Model 700FC

FDA 510(k) K052899 · Genesee Biomedical, Inc.

Substantially Equivalent

510(k) numberK052899

Submission

Device name
Ats Simulus Annuloplasty Band, Model 700FC
Applicant
Genesee Biomedical, Inc.
Denver, CO, US
Received
October 14, 2005
Decision date
November 17, 2005
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

Other 510(k)s with product code KRH

510(k)DeviceApplicantDecision
K261707MEMO 4D Curve™ Semirigid mitral annuloplasty ringKRH · Special Corcym S.r.l.06/18/2026SE
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
K083683Ats Simulus Semi-Rigid Mitral Annuloplasty Ring, Model 800SCKRH · Special 02/25/2009SE

Questions and answers

When was Ats Simulus Annuloplasty Band, Model 700FC cleared by the FDA?

Ats Simulus Annuloplasty Band, Model 700FC (K052899) received a 510(k) decision of Substantially Equivalent on November 17, 2005, 34 days after the submission was received.

What is the product code of K052899?

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