Atlas FDA

Blazer Prime XP and IntellaTip MiFi XP

FDA premarket approval P020025/S124 · decided 2020-02-07

Approval details

PMA number
P020025
Supplement
S124
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Blazer Prime XP and IntellaTip MiFi XP
Generic name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant
Boston Scientific
Date received
2020-01-15
Decision date
2020-02-07
Days to decision
23 days
Decision code
OK30
Product code
OAD
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
Addition of BSC Heredia as an alternate supplier for the steering control wire sub-assembly.

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