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Squale ™
Cervical cages
CE
510(k)
- Self-rotating blocking system during impaction
- Anatomical design
- Simple and intuitive instrumentation only two impactors and shape distractors
- Design adapted to vertebral anatomy
- Tantalum markers for positioning and control
- Anti-migration grooves and spikes (on 14mm width only)
- Broad implant portfolio
- Tantalum markers for positioning and control.
- Anti-migration grooves.
- Self-rotating blocking system during impaction.
- Made in OXPEKK ® Radio-transparent for a better control of intra-cage fusion.
- Height: 4, 5, 6, 7, 8mm
- Depth: 13 and 14mm
- Width: 14, 17, 20mm
Materials
| Cage | Markers | Markers | |
|---|---|---|---|
| Materials | OX-PEKK® | Tantalum Ta | Titanium alloy Ti6Al4V |
| Standards | ASTM F2820 | ASTM F560 | ISO 5832-3 |
Range
| Height (mm) | Length 14 mm / Width 13 mm | Length 17 mm / Width 13 mm | Length 20 mm / Width 15 mm |
|---|---|---|---|
| 4 | x | x | x* |
| 5 | x | x | x |
| 6 | x | x | x |
| 7 | x | x | x |
| 8 | x* | x* | x* |
| 9 | x* | x* | x* |
Brochure request form
Orthopaedic and Spine Development (OSD)
Class IIb medical devices of Orthopaedic and Spine Development (OSD) are CE 0459 marked with GMED, according to Directive 93/42/EEC and its amendments.
Before using a product, please refer to the instructions for use and the operative technique. Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.
Before using a product, please refer to the instructions for use and the operative technique. Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.
Implanet
Class IIb medical devices of Implanet are CE 0459 marked with GMED, according to Directive 93/42/EEC and its amendments.
Before using a product, please refer to the instructions for use and the operative technique. Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.
Before using a product, please refer to the instructions for use and the operative technique. Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.
Class II medical devices of Implanet are 510(k) cleared.
Federal Law restricts this device to sale by or on the order of a physician.
Before using a product, please refer to the instructions for use and the operative/surgical technique.
Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.va
Federal Law restricts this device to sale by or on the order of a physician.
Before using a product, please refer to the instructions for use and the operative/surgical technique.
Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.va
