510(k) K960766

Device
MEADOX MEDICALS, INC. EXPANDED PTFE VASCULAR GRAFT
Applicant
MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP.
510(k) number
K960766
Product code
DYF  
Decision
Se Subject To Tracking Reg (ST)
Decision date
1997-03-19
Date received
1996-02-26
Regulation
870.3450
Classification name
Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
STEPHEN B ANDERSON
Address
112 Bauer Dr. Oakland NJ US 07436 07436

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DYF  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K004012IMPRA CARBOFLO EPTFE VASCULAR GRAFTSImpra, Inc.2001-05-14
K000504ADVANTA SUPER SOFT GRAFTAtrium Medical Corp.2000-03-01
K992958ADVANTA GRAFT (<6MM)Atrium Medical Corp.1999-10-01
K991683PTFE RINGED GORE-TEX VASCULAR GRAFTW. L. Gore & Associates, Inc.1999-09-08
K992441ADVANTA GRAFTAtrium Medical Corp.1999-08-20
K984183PERMA-PASS VASCULAR GRAFT, 5T GRAFT,MODEL 31451Possis Medical, Inc.1999-02-01
K983769DISTAFLO BYPASS GRAFTImpra, Inc.1998-12-15
K981076VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFTImpra, Inc.1998-05-07
K964877IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFTImpra, Inc.1997-03-20
K955533DIASTAT VASCULAR ACCESS GRAFTW. L. Gore & Associates, Inc.1996-05-15
K953287DIASTAT VASCULAR ACCESS GRAFTW. L. Gore & Associates, Inc.1995-10-06
K944844BAXTER REINFORCED EXPANDED PTFE STEPPED VASCULAR GRAFTBaxter Healthcare Corp1995-03-31
K933391ATRIUM'S HYBRID PTFEAtrium Medical Corp.1994-12-15
K940824DIASTAT(TM) VASCULAR ACCESS GRAFT/CLASS IIIW. L. Gore & Associates, Inc.1994-05-04
K934726FEP RINGED GORE-TEX VASCULAR GRAFTW. L. Gore & Associates, Inc.1993-12-08

Legacy Summary#

summary

FDA Review#

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