IN-DATE
2990832: Medtronic Capstone Spinal System, PEEK 8mm x 32mm
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| Price: | $234.50 $46.90 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 2 box of 1 |
| Status: | expired |
| Express: | Need it tomorrow? Order in next 12 hours 15 minutes and choose overnight shipping at checkout for Monday delivery. If you require Saturday delivery, please call to determine if it is available in your area - 888-416-2409. |
Additional Details
Medtronic CAPSTONE® PEEK Interbody Spacer
The Medtronic CAPSTONE® PEEK Interbody Spacer is an implantable cage for lumbar interbody fusion, including posterior lumbar interbody fusion (PLIF) and transforaminal lumbar interbody fusion (TLIF). Available in multiple sizes, the spacer accommodates autogenous bone graft and provides support between lumbar or lumbosacral vertebral bodies during fusion.
- Manufacturer: Medtronic
- Product Name: CAPSTONE® PEEK Interbody Spacer
- Product Family: CAPSTONE® Spinal System
- Device Type: Interbody fusion cage
- Material: Polyetheretherketone (PEEK) with tantalum markers
- Configuration: Multiple implant heights and lengths
- Clinical Application: Interbody fusion with autogenous bone graft for degenerative disc disease
- Procedure Types: PLIF and TLIF
- Anatomical Application: Lumbar and lumbosacral spine, at one or two levels from L2 to S1
- Specialty: Orthopedic Surgery and Neurosurgery
- Fixation: Requires supplemental fixation instrumentation
- Implantable: Yes
- Single-Use: Yes
Features
- Open internal space accommodates autogenous bone graft.
- Tantalum markers enable radiographic visualization.
- Convex profile accommodates vertebral anatomy.
- Bullet-shaped tip facilitates insertion and distraction.
- Surface teeth help resist expulsion.
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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