Atlas FDA

TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™

FDA premarket approval P130026/S077 · decided 2022-08-17

Approval details

PMA number
P130026
Supplement
S077
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
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
2021-12-03
Decision date
2022-08-17
Days to decision
257 days
Decision code
APPR
Product code
OAE
Advisory committee
Cardiovascular
Expedited review
No
Location
St. Paul, MN
Statement
Approval for protocol (ABT-CIP-10436 Version A) for the post-approval study (PAS) protocol.

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