leaflet-cap-lumbar-cages

Product catalog summary

Indications: The lumbar interbody fusion devices are indicated for recurrence of discal hernia, degenerative discopathy with instability, restoration of discal height, and Grade I spondylolisthesis. These devices are designed for treating degenerative disc diseases and instabilities at any level between L1 and S1.

Design and Features: The devices are biconvex for optimal bone contact and come in standard or lordotic shapes. They include bone-hugging serrations, a large bone graft area, radio-opaque markers, and a threaded anterior part for stable impaction. They are available in a wide range of sizes and angles.

Materials and Approaches: The devices are made from PEEK OPTIMA® LT1 and Titanium TA6V. They can be approached posteriorly (PLIF) or postero-laterally (TPLIF). Length options are 20 or 25 mm, with heights ranging from 8 to 14 mm and angles of 0°, 4°, or 8°.

Product Variants: The document lists several variants including the Posterior cage CAP, Posterior cage CAP-LB, Postero-lateral cage, and Posterior cage Titanium.

Regulatory Information: CAP is a CE-marked medical device of class IIb (implants) and class I (instruments), manufactured by hpi. Conformity evaluation was conducted by SGS n°1639. Product availability may vary by country and market.

Instructions for Use: This document is intended for healthcare professionals. It is crucial to read the instructions carefully before any surgical procedure. In France, CAP is covered by the Assurance Maladie.

Instruments: The document mentions instruments such as a removable handle, distractor, reamer, and impactor with holder.

Catalog excerpts

CAP Cages intersomatiques lombaires Lumbar interbody fusion devices Cage intersomatique lombaire conçue pour le traitement des pathologies discales dégénératives et d’instabilités à tout niveau entre L1-S1. Biconvexe Contact osseux optimal Contour standard ou lordosant Stries de stabilisation Bone-hugging serrations Lumbar interbody fusion device designed for the treatment of degenerative disc diseases and instabilities at any level between L1 and S1. Large espace de greffe osseuse Témoins radio-opaques Partie antérieure taraudée Biconvexe Optimal bone contact Standard or lordotic shape Matière/Material: PEEK OPTIMA® LT1/TITANE TA6V - TITANIUM TA6V Approche/Approach: postérieure /posterior PLIF Postero-lateral TPLIF Large bone graft area Radio-opaque markers Threaded anterior part Impaction stable Large gamme Stable impaction Wide range Indications • Récidive de hernies discales • Discopathies dégénératives avec instabilité • estaurer la hauteur discale R • Spondylolysthesis Grade I • Recurrence of discal hernia • Degenerative discopathy with instability • Restore discal hei

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Implants CAP lombaires / Lumbar PLIF Cage postérieure CAP Posterior cage CAP TPLIF Cage postéro-latéral Postero-lateral cage H PLIF Cage postȃrieure Titane Posterior cage Titanium PLIF Cage postɃrieure CAP-LB Posterior cage CAP-LB L : Longueur/Length: 20 ou/or 25 mm H : Hauteur/Height: 8, 9, 10, 11, 12 mmд A : Angle: 0Ȃ, 4Ђ Distracteur - Distractor Impacteur Ѓ prhension Impactor with holder PoignɃe amovible Removable handle AlɃsoir - Reamer CAP est un dispositif mɃdical marquɃ CE de classe IIb (implants), classe I (instruments), fabriquɃ par hpi et dont lɢévaluation de la confomité a été réalisée...

Open the catalog to page 2

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*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.

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