Atlas FDA

Linx Reflux Management System

FDA premarket approval P100049/S028 · decided 2019-12-10

Approval details

PMA number
P100049
Supplement
S028
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Linx Reflux Management System
Generic name
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX
Applicant
Torax Medical
Date received
2019-10-25
Decision date
2019-12-10
Days to decision
46 days
Decision code
OK30
Product code
LEI
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Cincinnati, OH
Statement
Implementation of a new automatic measuring system and measuring test method.

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