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DTRAX Cervical Cage-T

Providence Medical Technology, Inc. · Model PD-31-100 · UDI-DI 10852776006017

ODP Prescription

510(k) clearances

1,116

Adverse events (3 deaths)

Recalls

344

Facilities

Description

The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level.

Recalls

Date	Firm	Reason
2025-11-03	Orthofix U.S. LLC	Labeling contains claims that are not consistently present.
2025-11-03	Orthofix U.S. LLC	Labeling contains claims that are not consistently present.
2023-07-12	Medicrea International	There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
2023-07-12	Medicrea International	There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
2023-07-12	Medicrea International	There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
2020-09-30	XTANT Medical	Cervical Implants contain a label that incorrectly identifies the grade of titanium used.
2013-10-07	RTI Surgical, Inc.	As the result of a recent internal review of regulatory documents, we have determined that the 10 mm x 12 mm Webless C-Plus implants were incorrectly documented as meeting the requ
2013-02-05	SpineNet	The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to
2012-06-15	Exactech, Inc.	Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe Locking Screws, Equinoxe Compression Screw Kits, Equinoxe Fracture Adapter Tray Screws, and Octane-C Inter
2011-09-23	Synthes USA (HQ), Inc.	LABELING CORRECTION - Following review of labeling and promotional materials associated with the Zero-P Implant system, it was found that the materials reference a study where PEEK

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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.