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ESSENTIO™ SR, ESSENTIO DR, ESSENTIO EL DR, PROPONENT™ SR, PROPONENT DR, PROPONENT EL DR, ACCOLADE™ SR, ACCOLADE DR, ACCO

FDA premarket approval N970003/S276 · decided 2022-09-27

Approval details

PMA number
N970003
Supplement
S276
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ESSENTIO™ SR, ESSENTIO DR, ESSENTIO EL DR, PROPONENT™ SR, PROPONENT DR, PROPONENT EL DR, ACCOLADE™ SR, ACCOLADE DR, ACCO
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Boston Scientific Corp
Date received
2022-09-20
Decision date
2022-09-27
Days to decision
7 days
Decision code
OK30
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
Implement an automatic handling system for the helium leak test process.

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510(k) clearances by this applicant

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EndoVive Initial Placement Standard PEG Kit with ENFit Connector, EndoVive Initial Placement Safety PEG Kit with ENFit Connector (K150679)Boston Scientific Corp2015-05-29
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