Atlas FDA

TOPS™ System

FDA premarket approval P220002/S006 · decided 2025-03-25

Approval details

PMA number
P220002
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
TOPS™ System
Generic name
Prosthesis, posterior spinal elements
Applicant
Premia Spine, Ltd.
Date received
2024-12-26
Decision date
2025-03-25
Days to decision
89 days
Decision code
APPR
Product code
QWK
Advisory committee
Orthopedic
Expedited review
No
Location
Netanya
Statement
Approval for the use of additional pedicle screw components (CD Horizon Solera Ø6.5-7.5mm non-cannulated, multi-axial pedicle screws with lengths from 25-60mm manufactured by Medtronic Sofamor Danek USA, Inc.) with the TOPS™ System

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510(k) clearances by this applicant

RecordFirmDate
ProMIS Extension Rod System (K232719)Premia Spine, Ltd.2023-11-21
ProMIS™ Fixation System (K231844)Premia Spine, Ltd.2023-07-07
Premia Spine XL Instruments (K191854)Premia Spine, Ltd.2019-10-08
VersaLink™ Fixation System (K182598)Premia Spine, Ltd.2018-11-13
ProMIS™ Fixation System (K170061)Premia Spine, Ltd.2017-02-02
ProMIS Fixation System (K150380)Premia Spine, Ltd.2015-07-17