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ostaPek® interbody fusion Erriva™ ELIF TLIF

ostaPek® transforaminal lumbar interbody fusion cages.

The ostaPek® Erriva™ 3 cage is the latest design of the Coligne transforaminal lumbar interbody fusion cages. Gentle bulleting and tapering of the ostaPek® Erriva™ 3 cage combined with ventral placement allows sagittal correction after implantation through a small, foraminal annulotomy. A specifically engineered interface with the cage inserter provides strength and control during implantation. Final positioning of the cage is achieved with easy-to-use instrumentation designed for this type of cage.

Clinically used in Europe since 2005. Cleared by the FDA under MAX code in 2018 510(k) K181963.

Erriva™ cages and instruments are patented, have been developed in the USA and are manufactured in Switzerland.

The ostaPek® Interbody Fusion Cages system is indicated for use as an intervertebral body fusion device in skeletally mature patients at one or two contiguous levels of the sacro-lumbar spine (L2-S1) to facilitate fusion in case of degenerative disc disease (DDD) defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. DDD patients may also have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The ostaPek erriva Interbody Fusion Cages are placed via a posterior or postero-lateral approach using autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft. The ostaPek Interbody Fusion Cages are to be used with supplemental fixation cleared by the FDA for use in the lumbar spine, i.e. GII System. Patients should have at least six weeks of non-operative treatment prior to surgery. Patients with previous non-fusion spinal surgery at involved level may be treated with the device.

Examples of indications discogenic lombalgy of 1 or 2 levels with foraminal stenosis, second recidive of foraminal disc herniation.

The Erriva™ cage is available in different lengths 4 heights.

For complete details on the use of the Erriva™ system refer to the valid Information for Use.

Peer-reviewed clinical publications on the ELIF system.