Atlas FDA

TOPS™ System

FDA premarket approval P220002/S003 · decided 2023-10-27

Approval details

PMA number
P220002
Supplement
S003
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
2023-09-28
Decision date
2023-10-27
Days to decision
29 days
Decision code
OK30
Product code
QWK
Advisory committee
Orthopedic
Expedited review
No
Location
Netanya
Statement
Change to introduce a semi-automated machine for the insertion of the Polycarbonate Urethane (PcU) Plug, adjustment to the Leak Detection Machine and change to the pedicle screw body surface blasting of 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