Atlas FDA

SpineSeal Spine Sealant

FDA premarket approval P240027/S002 · decided 2025-06-04

Approval details

PMA number
P240027
Supplement
S002
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
SpineSeal Spine Sealant
Generic name
Sealant, dural
Applicant
Pramand, LLC
Date received
2025-03-06
Decision date
2025-06-04
Days to decision
90 days
Decision code
APPR
Product code
NQR
Advisory committee
Neurology
Expedited review
No
Location
Bedford, MA
Statement
Approval for a change to the syringes that contain the precursor and diluent solution components.

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