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POSSIS PERMA-SEAL DIALYSIS ACCESS GRAFT

FDA premarket approval P980017/S001 · decided 1999-03-24

Approval details

PMA number
P980017
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
POSSIS PERMA-SEAL DIALYSIS ACCESS GRAFT
Applicant
Possis Medical, Inc.
Date received
1998-12-29
Decision date
1999-03-24
Days to decision
85 days
Decision code
APPR
Advisory committee
Cardiovascular
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for extending the shelf life of the device from 3 to 6 years, and is indicated for use as a subcutaneous arteriovenous shunt graft to provide immediate and subsequent chronic blood access for high-efficiency hemodialysis in patients who meet one or more of the following conditions: 1)central venous cannulation is deemed hazardous or is technically unabailable; 2) are being maintained on chronic anticoagulation or antithrombotic therapy; and/or 3) are morbidly obese.

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510(k) clearances by this applicant

RecordFirmDate
ANGIOJET ULTRA AVX THROMBECTOMY SET (K133629)Possis Medical, Inc.2014-02-14
ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETS (K091593)Possis Medical, Inc.2009-06-22
ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL 106552-001, ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040-001 (K090253)Possis Medical, Inc.2009-04-08
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 (K082382)Possis Medical, Inc.2008-12-12
MODIFICATION TO FETCH ASPIRATION CATHETER (K081989)Possis Medical, Inc.2008-09-26
GUARDDOG OCCLUSION GUIDEWIRE, INFLATION DEVICE (K081454)Possis Medical, Inc.2008-06-13
ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608 (K080806)Possis Medical, Inc.2008-04-04
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 (K073441)Possis Medical, Inc.2008-01-24