Duran Flexible Annuloplasty Ring Model Number H608H
FDA 510(k) K980534 · The Heart Valve Div. Medtronic Cardiovascular Surg
510(k) numberK980534
Submission
- Device name
- Duran Flexible Annuloplasty Ring Model Number H608H
- Applicant
- The Heart Valve Div. Medtronic Cardiovascular Surg
Irvine, CA, US - Received
- February 11, 1998
- Decision date
- April 30, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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) | Device | Applicant | Decision |
|---|---|---|---|
| K261707 | MEMO 4D Curve Semirigid mitral annuloplasty ringKRH · Special | Corcym S.r.l. | 06/18/2026SE |
| K260498 | TriMemo SEMIRIGID ANNULOPLASTY RINGKRH · Abbreviated | Corcym S.r.l. | 04/14/2026SE |
| K253232 | Seguin Annuloplasty RingKRH · Special | Abbott Medical | 10/29/2025SE |
| K251982 | Edwards MC3 Tricuspid annuloplasty ring (4900)KRH · Abbreviated | Edwards Lifesciences, LLC | 09/23/2025SE |
| K251688 | Carpentier-Edwards Physio Annuloplasty Ring (4450)KRH · Abbreviated | Edwards Lifesciences, LLC | 09/17/2025SE |
| K250859 | TransForm McCarthy Mitral Annuloplasty Ring (TF)KRH · Traditional | Genesee Biomedical, Inc. | 07/25/2025SE |
| K232599 | TransForm McCarthy Mitral Annuloplasty Ring (TF)KRH · Traditional | Genesee Biomedical, Inc. | 04/09/2024SE |
| K230679 | WellsForm Tricuspid Annuloplasty Band (WF)KRH · Traditional | Genesee Biomedical, Inc. | 05/26/2023SE |
| K230318 | Memo 3D Semirigid Annuloplasty Ring; Memo 3D ReChord Semirigid Annuloplasty Ring; Memo…KRH · Traditional | Corcym S.r.l. | 04/07/2023SE |
| K202253 | TruForm Sievers Annuloplasty RingKRH · Traditional | Genesee Biomedical, Inc. | 10/06/2020SE |
More from Genesee Biomedical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K960356 | Posterior Annuloplasty Band (Model 607)KRH · Traditional | 08/27/1996ST |
| K944956 | Unipolar Pediatric Temporary Pacing Lead, Model 6491LDF · Traditional | 07/14/1995SE |
| K922269 | Unipolar Temporary Myocardial Pacing Wire, 6493LDF · Traditional | 11/23/1992SE |
| K914602 | Duran Flex Annuloplasty Ring/Obtur H601H, ModifiedKRH · Traditional | 11/22/1991SE |
Questions and answers
When was Duran Flexible Annuloplasty Ring Model Number H608H cleared by the FDA?
Duran Flexible Annuloplasty Ring Model Number H608H (K980534) received a 510(k) decision of Substantially Equivalent on April 30, 1998, 78 days after the submission was received.
What is the product code of K980534?
The FDA product code is KRH – Ring, Annuloplasty, a Class II (moderate risk) device regulated under 21 CFR 870.3800.