Atlas FDA

TRYTON Side Branch Stent

FDA premarket approval P150039/S001 · decided 2017-07-13

Approval details

PMA number
P150039
Supplement
S001
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
TRYTON Side Branch Stent
Generic name
STENT, CORONARY
Applicant
Poseidon Medical, Inc.
Date received
2017-03-13
Decision date
2017-07-13
Days to decision
122 days
Decision code
APPR
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Pembroke Pines, FL
Statement
Approval of the protocol for the post-approval study (PAS) protocol.

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