Atlas FDA

ON-X PROSTHETIC HEART VALVE

FDA premarket approval P000037/S028 · decided 2013-02-13

Approval details

PMA number
P000037
Supplement
S028
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ON-X PROSTHETIC HEART VALVE
Generic name
HEART-VALVE, MECHANICAL
Applicant
On-X Life Technologies, Inc.
Date received
2012-06-28
Decision date
2013-02-13
Days to decision
230 days
Decision code
APPR
Product code
LWQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Kennesaw, GA
Statement
APPROVAL FOR A MODIFIED AORTIC SEWING CUFF AS AN EXTENSION TO THE LINE OF AVAILABLE VALVES; THE REQUEST APPLIED TO THE AORTIC SIZES OF 19, 21, 23, 25, AND 27/29 MM. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME ON-X AORTIC PROSTHETIC HEART VALVE WITH ANATOMIC SEWING RING, AND WILL BE GIVEN THE MODEL DESIGNATIONS OF ONXAN (STANDARD VALVE HOLDER) AND ONXANE (EXTENDED VALVE HOLDER).

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510(k) clearances by this applicant

RecordFirmDate
CHORD-X PRE-MEASURED LOOPS FOR MITRAL CHORDAL REPLACEMENT (K141060)On-X Life Technologies, Inc.2014-06-06