Atlas FDA

TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™

FDA premarket approval P130026/S087 · decided 2023-08-17

Approval details

PMA number
P130026
Supplement
S087
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™
Generic name
Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
Applicant
St Jude Medical
Date received
2023-07-25
Decision date
2023-08-17
Days to decision
23 days
Decision code
OK30
Product code
OAE
Advisory committee
Cardiovascular
Expedited review
No
Location
St. Paul, MN
Statement
Additional equipment inspection in the Bi-Directional handle assembly manufacturing procedure.

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