Atlas FDA

Apollo™ Onyx™ Delivery Micro Catheter 1.5 cm, Apollo™ Onyx™ Delivery Micro Catheter 3.0 cm

FDA premarket approval P030004/S031 · decided 2024-04-16

Approval details

PMA number
P030004
Supplement
S031
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Apollo™ Onyx™ Delivery Micro Catheter 1.5 cm, Apollo™ Onyx™ Delivery Micro Catheter 3.0 cm
Generic name
Agent, injectable, embolic
Applicant
Ev3 Neurovascular
Date received
2024-03-19
Decision date
2024-04-16
Days to decision
28 days
Decision code
OK30
Product code
MFE
Advisory committee
Neurology
Expedited review
No
Location
Irvine, CA
Statement
approval for the additional supplier for the Hub used in the delivery catheter.

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
MERIDIAN GUIDEWIRE (K093681)Ev3 Neurovascular2010-01-26
HYPERGLIDE OCCLUSION BALLOON SYSTEM, HYPERFORM OCCLUSION BALLOON SYSTEM, MODEL 104-4112, 104-4113, 104-4127,104-4132,104 (K091458)Ev3 Neurovascular2009-10-15
HYPERGLIDE OCCLUSION BALLOON SYSTEM, MODEL 104-4310, 104-4315 (K092495)Ev3 Neurovascular2009-09-22