Atlas FDA

TOPS™ System

FDA premarket approval P220002/S008 · decided 2025-05-29

Approval details

PMA number
P220002
Supplement
S008
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TOPS™ System
Generic name
Prosthesis, posterior spinal elements
Applicant
Premia Spine, Ltd.
Date received
2025-05-02
Decision date
2025-05-29
Days to decision
27 days
Decision code
OK30
Product code
QWK
Advisory committee
Orthopedic
Expedited review
No
Location
Netanya
Statement
qualification of an additional VST leakage testing machine for the TOPS™ System implant at the Ramat Poleg, Netanya, Israel facility

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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