Atlas FDA

GORE HELEX SEPTAL OCCLUDER

FDA premarket approval P050006/S027 · decided 2012-05-30

Approval details

PMA number
P050006
Supplement
S027
Supplement type
30-Day Notice
Trade name
GORE HELEX SEPTAL OCCLUDER
Generic name
Transcatheter septal occluder
Applicant
W. L. Gore & Associates, Inc.
Date received
2012-05-01
Decision date
2012-05-30
Days to decision
29 days
Decision code
OK30
Product code
MLV
Advisory committee
Cardiovascular
Expedited review
No
Location
Phonix, AZ
Statement
CHANGE TO THE AUTOMATED MANUFACTURING AND TESTING DOCUMENTATION PROCESS.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
GORE® Tri-Lobe Balloon Catheter (K250410)W. L. Gore & Associates, Inc.2025-06-02
GORE® PROPATEN® Vascular Graft (K240083)W. L. Gore & Associates, Inc.2024-03-01
GORE® PROPATEN® Vascular Graft (K232312)W. L. Gore & Associates, Inc.2024-01-09
GORE® ACUSEAL Vascular Graft (K233551)W. L. Gore & Associates, Inc.2023-12-19
GORE® ACUSEAL Vascular Graft (K231505)W. L. Gore & Associates, Inc.2023-06-23
GORE BIO-A Tissue Reinforcement (K191773)W. L. Gore & Associates, Inc.2019-07-31
GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement (K181940)W. L. Gore & Associates, Inc.2018-08-17
GORE ENFORM Biomaterial (K173333)W. L. Gore & Associates, Inc.2018-04-05