Atlas FDA

Tendril MRI Lead

FDA premarket approval P140033/S040 · decided 2018-10-31

Approval details

PMA number
P140033
Supplement
S040
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Tendril MRI Lead
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
ABBOTT MEDICAL
Date received
2018-10-02
Decision date
2018-10-31
Days to decision
29 days
Decision code
OK30
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
Update to the cleaning process for incoming components.

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