6661125: Medtronic Spinal Interbody Fusion Device, 25mm x 11mm

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| Price: | $117.00 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 1 box of 1 |
| Status: | expired |
AccessGUDID Info
- FDA Product Code: MAX
- FDA Product Code Name: Intervertebral fusion device with bone graft, lumbar
- GMDN Term Code: 60762
- GMDN Term Name: Polymeric spinal interbody fusion cage
- GMDN Term Description: A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
Manufacturer
Medtronic’s former Minimally Invasive Therapies Group (MITG), now part of the Surgical and Endoscopy Operating Units within the Medical Surgical Portfolio, focuses on advanced technologies that support minimally invasive procedures across general, bariatric, colorectal, and thoracic surgery. The portfolio includes a wide range of surgical stapling systems like the Signia and Endo GIA platforms, energy devices such as the LigaSure vessel sealing system and Valleylab electrosurgical generators, as well as a robust line of trocars, sutures, and advanced instrumentation. MITG also includes market-leading solutions in gastrointestinal diagnostics and respiratory monitoring, including the Bravo pH monitoring system and the Puritan Bennett ventilators. Medtronic’s innovations in this space aim to improve surgical precision, reduce complications, and enhance recovery through technology-driven, value-based care.
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