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FFX 13x3.5

SC MEDICA · Model 57.000.60S · UDI-DI 03770019503058

MRW Prescription

510(k) clearances

105

Adverse events

Recalls

100

Facilities

Description

The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.

Recalls

Date	Firm	Reason
2021-04-27	Medtronic Sofamor Danek USA, Inc	Product is impacted by a thread profile defect due to a manufacturing issue.
2011-06-07	Osteomed, Lp	Two of the Implant Driver Assembly tips were reported to break during surgery.
2011-03-15	Interventional Spine Inc	This recall has been initiated due to Pull Pins that may disengage from the Facet Screw during the compression step, requiring that compression be completed with a device driver ra
2011-03-15	Interventional Spine Inc	This recall has been initiated due to Pull Pins that may disengage from the Facet Screw during the compression step, requiring that compression be completed with a device driver ra

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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.