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AnyPlus Spinal Fixation System

GS Medical Co., Ltd. · Model 0912-4535 · UDI-DI 08806378317168

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

Description

The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous 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.