Atlas FDA

COBRA PzF NanoCoated Coronary Stent System

FDA premarket approval P160014/S002 · decided 2018-07-12

Approval details

PMA number
P160014
Supplement
S002
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
COBRA PzF NanoCoated Coronary Stent System
Generic name
STENT, CORONARY
Applicant
Celonova Biosciences, Inc.
Date received
2018-06-12
Decision date
2018-07-12
Days to decision
30 days
Decision code
OK30
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
San Antonio, TX
Statement
Change to the manufacturer of the adhesion promoter used in the coating process of the COBRA PzF stent.

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
EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED) MICROSPHERES, ONCOZENE MICROSPHERES (K141209)Celonova Biosciences, Inc.2014-08-07
EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED) MICROSPHERES (K133447)Celonova Biosciences, Inc.2014-02-24
EMBOZENE MICROSPHERES (K132675)Celonova Biosciences, Inc.2013-10-03
ONCOZENE MICROSPHERES 40UM, 2ML, ONCOZENE MICROSPHERES 75UM, 2ML, ONCOZENE MICROSPHERES 100UM, 2ML, ONCOZENE MICROSPHERE (K130307)Celonova Biosciences, Inc.2013-03-04
EMBOZENE MICROSPHERES (K073417)Celonova Biosciences, Inc.2008-12-15