Two-piece prosthetic valve

1. A two-piece prosthetic valve assembly, consisting of:

a bioremodelable first conduit member having first and second ends, and an internal lumen, said first conduit member lumen having an inner surface; and

a separate bioremodelable second conduit member having first and second ends, and an internal lumen,

said first and second conduit members comprising an extracellular matrix (ECM) material from a mammalian tissue source, said tissue source comprising small intestine submucosa (SIS),

said first end of said first conduit member being configured to receive said second end of said second conduit member therein, wherein said second end of said second conduit member is disposed in said first end of said first conduit member, said second end of said second conduit member being directly attached to said first conduit member lumen inner surface at a first commissure connection point, wherein said first conduit member lumen and said second conduit member lumen are in communication, and wherein a first valve leaflet is formed by said second end of said second conduit member within said first conduit member lumen, said first valve leaflet being configured to selectively restrict fluid flow through said two-piece valve assembly, and

wherein, following attachment of said valve assembly to a cardiovascular vessel, said first and second conduit members are remodeled by cardiovascular tissue to form an integral valve member comprising remodeled cardiovascular tissue.

2. The two-piece valve assembly of claim 1 , wherein said second end of said second conduit member is attached to said first conduit member lumen inner surface at two commissure connection points, and wherein first and second valve leaflets are formed within said first conduit member lumen.

3. The two-piece valve assembly of claim 1 , wherein said second end of said second conduit member is attached to said first conduit member lumen inner surface at three commissure connection points, and wherein first, second and third valve leaflets are formed within said first conduit member lumen.

4. The two-piece valve assembly of claim 1 , wherein said attached first and second conduit members have substantially coincident longitudinal axes.

5. The two-piece valve assembly of claim 4 , wherein said three commissure connection points are positioned substantially within a common plane, said common plane being substantially perpendicular to said substantially coincident longitudinal axes of said first and second conduit members.

6. The two-piece valve assembly of claim 1 , wherein said first end of said first member is sealably attached to said second end of said second member.

7. The two-piece valve assembly of claim 1 , wherein said tissue source is selected from the group consisting of urinary bladder submucosa (UBS), stomach submucosa (SS), central nervous system tissue, epithelium of mesodermal origin, dermal extracellular matrix, subcutaneous extracellular matrix, gastrointestinal extracellular matrix, tissue surrounding growing bone, placental extracellular matrix, ornamentum extracellular matrix, cardiac extracellular matrix, kidney extracellular matrix, pancreas extracellular matrix, lung extracellular matrix, and combinations thereof.

8. The two-piece valve assembly of claim 1 , wherein said ECM material further includes an additional pharmacological agent.

9. The two-piece valve assembly of claim 8 , wherein said pharmacological agent comprises an anti-inflammatory.

10. The two-piece valve assembly of claim 8 , wherein said pharmacological agent comprises a statin.

11. The two-piece valve assembly of claim 10 , wherein said statin is selected from the group consisting of atorvastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin and simvastatin.

12. The two-piece valve assembly of claim 8 , wherein said pharmacological agent comprises a growth factor.

13. The two-piece valve assembly of claim 12 , wherein said growth factor is selected from the group consisting of a platelet derived growth factor (PDGF), epidermal growth factor (EGF), transforming growth factor alpha (TGF-alpha), transforming growth factor beta (TGF-beta), fibroblast growth factor-2 (FGF-2), basic fibroblast growth factor (bFGF), vascular epithelial growth factor (VEGF), hepatocyte growth factor (HGF), insulin-like growth factor (IGF), nerve growth factor (NGF), platlet derived growth factor (PDGF), tumor necrosis factor alpha (TNA-alpha), and placental growth factor (PLGF).

14. The two-piece valve assembly of claim 8 , wherein said pharmacological agent comprises an anti-arrhythmic agent.

15. The two-piece valve assembly of claim 14 , wherein said anti-arrhythmic agent is selected from the group comprising quinidine, procainamide, disopyramide, lidocaine, phenyloin, mexiletine, flecamide, propafenone, moricizine, propranolol, esmolol, timolol, metoprolol, atenolol, amiodarone, sotalol, ibutilide, dofetilide, verapamil, diltiazem, adenosine and digoxin.

16. A two-piece prosthetic valve assembly, consisting of:

a bioremodelable first conduit member having first and second ends, and an internal lumen, said first conduit member lumen having an inner surface; and

a separate bioremodelable second conduit member having first and second ends, and an internal lumen,

said first and second conduit members comprising an extracellular matrix (ECM) material from a mammalian tissue source, said tissue source comprising small intestine submucosa (SIS), said SIS further comprising an exogenously added pharmacological agent, said pharmacological agent comprising a statin selected from the group consisting of atorvastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin and simvastatin,

said first end of said first conduit member being configured to receive said second end of said second conduit member therein, wherein said second end of said second conduit member is disposed in said first end of said first conduit member, said second end of said second conduit member being directly attached to said first conduit member lumen inner surface at a first commissure connection point, wherein said first conduit member lumen and said second conduit member lumen are in communication, and wherein a first valve leaflet is formed by said second end of said second conduit member within said first conduit member lumen, said first valve leaflet being configured to selectively restrict fluid flow through said two-piece valve assembly, and

wherein, following attachment of said valve assembly to a cardiovascular vessel, said first and second conduit members are remodeled by cardiovascular tissue to form an integral valve member comprising remodeled cardiovascular tissue.

17. The two-piece valve assembly of claim 16 , wherein said second end of said second conduit member is attached to said first conduit member lumen inner surface at two commissure connection points, and wherein first and second valve leaflets are formed within said first conduit member lumen.

18. The two-piece valve assembly of claim 16 , wherein said second end of said second conduit member is attached to said first conduit member lumen inner surface at three commissure connection points, and wherein first, second and third valve leaflets are formed within said first conduit member lumen.

19. The two-piece valve assembly of claim 16 , wherein said pharmacological agent comprises an anti-arrhythmic agent selected from the group comprising quinidine, procainamide, disopyramide, lidocaine, phenyloin, mexiletine, flecamide, propafenone, moricizine, propranolol, esmolol, timolol, metoprolol, atenolol, amiodarone, sotalol, ibutilide, dofetilide, verapamil, diltiazem, adenosine and digoxin.