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FDA 510(k)

CG FUTURE ANNULOPLASTY BAND

K-Number: K052860 · 2005-11-10

ApplicantMedtronic Heart Valves
Decision Date2005-11-10
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CG FUTURE ANNULOPLASTY BAND is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Heart Valves. It received FDA 510(k) clearance on 2005-11-10 under 510(k) number K052860. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CG FUTURE ANNULOPLASTY BAND?

CG FUTURE ANNULOPLASTY BAND is a medical device that received FDA 510(k) clearance on 2005-11-10. The listed applicant is Medtronic Heart Valves. The 510(k) number is K052860.

When did CG FUTURE ANNULOPLASTY BAND receive FDA 510(k) clearance?

CG FUTURE ANNULOPLASTY BAND received FDA 510(k) clearance on 2005-11-10, under 510(k) number K052860.

Who is the listed applicant for CG FUTURE ANNULOPLASTY BAND?

The FDA 510(k) record lists Medtronic Heart Valves as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CG FUTURE ANNULOPLASTY BAND?

The FDA product code for CG FUTURE ANNULOPLASTY BAND is KRH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medtronic Heart Valves as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K052970SIMPLICI-T ANNULOPLASTY SYSTEMK032810DURAN BAND (MODEL H607H), DURAN RING (MODEL 610R), DURAN BAND (MODEL 610B), DURAN ANCORE RING (MODEL 620R), DURAN ANCORE

Related Devices (Code: KRH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261707MEMO 4D Curve™ Semirigid mitral annuloplasty ringCorcym S.r.l.K260498TriMemo™ SEMIRIGID ANNULOPLASTY RINGCorcym S.r.l.K253232Seguin Annuloplasty RingABBOTT MEDICALK251982Edwards MC3 Tricuspid annuloplasty ring (4900)Edwards Lifesciences, LLCK251688Carpentier-Edwards Physio Annuloplasty Ring (4450)Edwards Lifesciences, LLCK250859TransForm McCarthy Mitral Annuloplasty Ring (TF)Genesee Biomedical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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