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ProMIS™ Fixation System

PREMIA SPINE LTD · Model 86258 · UDI-DI 07290014080119

MNINKBMNH Prescription
3
510(k) clearances
3,992
Adverse events (17 deaths)
213
Recalls
344
Facilities

Description

Pre Bent Rod Ø6.0x180mm Hex Edge The ProMIS Fixation System is designed to be implanted in the lumbar spine. The ProMIS Fixation System uses Polyaxial Head Pedicle Screws for fixation to the vertebrae.

Recalls

DateFirmReason
2026-02-18XTANT Medical Holdings, IncUnits from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
2023-07-12Medicrea InternationalThere is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
2018-07-05CTL Medical Corporationthe anti-toggle ring of the hex driver may separate from the driver shaft. If this occurs during surgery, the anti-toggle ring can be pressed into the pedicle screw head and cause
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.
2017-06-21Valorem Surgical LLCDevices are not consistent with Quality System Requirements.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.