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GSS Pedicle Screw System

GS Medical Co., Ltd. · Model GS0161-0075-M0 · UDI-DI 08806162184792

MNIMNH Prescription
1
510(k) clearances
3,989
Adverse events (17 deaths)
213
Recalls
343
Facilities

Description

"The GSS Pedicle Screw System is a top-loading multiple component, posterior spinal fixation system which consists of pedicle screws, rods, locking spacer, and a transverse (cross) linking mechanism. The GSS Pedicle Screw System will allow surgeons to build a spinal implant construct to stabilize and promote spinal fusion. The GSS Pedicle Screw System implant components are supplied non-sterile, single use and fabricated from titanium alloy (Ti-6AI-4V ELI) that conforms to ASTM F136. Various sizes of these implants are available. Specialized instruments are available for the application and removal of the GSS Pedicle Screw System. The GSS Pedicle Screw System is a pedicle screw system indicated for the treatment of severe Spondylolisthesis (Grade 3 and 4) of the L5-SI vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum) with removal of the implants after the attainment of a solid fusion."

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.