PMA P100044S021

Device
PROPEL AND PROPEL MINI SINUS IMPLANTS
Applicant
Intersect Ent.
PMA number
P100044
Supplement
S021
Product code
OWO
Decision date
2016-06-17
Classification
Drug-eluting Sinus Stent
Generic name
Drug-eluting sinus stent
Approval order statement
Modification of two packaging related processes: 1) the addition of an automated Desiccant Dispenser to automatically dispense the desiccants used in the manufacturing product packaging; and 2) the addition of a semi-automated Component Verification System for verifying the presence of components during packaging. These changes are being made to implement the addition of two new equipment systems to facilitate the conversion from manual to automated processes

Current openFDA PMA Record#

Device
PROPEL AND PROPEL MINI SINUS IMPLANTS
Applicant
Intersect Ent.
PMA number
P100044
Supplement
S021
Product code
OWO
Generic name
Drug-eluting sinus stent
Decision date
2016-06-17
Decision code
OK30
Date received
2016-05-18
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Modification of two packaging related processes: 1) the addition of an automated Desiccant Dispenser to automatically dispense the desiccants used in the manufacturing product packaging; and 2) the addition of a semi-automated Component Verification System for verifying the presence of components during packaging. These changes are being made to implement the addition of two new equipment systems to facilitate the conversion from manual to automated processes