Atlas FDA

Tula System

FDA premarket approval P190016/S008 · decided 2023-12-22

Approval details

PMA number
P190016
Supplement
S008
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Tula System
Generic name
Tympanostomy tube delivery product with drug
Applicant
Tusker Medical, Inc.
Date received
2023-06-30
Decision date
2023-12-22
Days to decision
175 days
Decision code
APPR
Product code
QJA
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Menlo Park, CA
Statement
Approval for the sterilization of the Gen 2 Tube Delivery System (TDS) at the new contract sterilizer, Sterigenics, located in Costa Rica

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510(k) clearances by this applicant

RecordFirmDate
Tula Tympanostomy Tube Delivery Device (K252436)Tusker Medical, Inc.2026-04-23