medical line

NG Bone

Extracellular Bone Matrix
Generic name:
extracellular bone matrix of porcine origin for guided tissue regeneration.

Composition/active substance:
Bone matrix composed of hydroxyapatite and collagen of porcine origin.

Presentations/models:

CodeParticle size
N210 - 1000 µm
N+294 - 840 µm
G1000 - 2000 µm
G+840 - 2000 µm
EG> 2000 µm

In presentations of 5 ml; 10 ml; 20 ml.
Cortico-cancellous blocks, boards and wedges.
Chips
Demineralized cortical sheets.

FEATURES
The extracellular bone matrix of porcine origin has a histological microstructure with interconnected pores similar to that of human bone, which allows penetration and cellular development of the patient’s bone tissue in a manner similar to normal autologous cancellous bone or from tissue bank.

With a high osteoconductive capacity and thanks to the presence of collagen, it also has osteoinductive capacity, which allows the repair and growth of tissue in the implanted area.
It offers the specialist surgeon the following properties:

Sterile, inert and biocompatible material.
Hydrophilic and easy to adapt to the implant site
CLINICAL INDICATIONS
Its use is indicated in the following cases:
Bone substitute in medical surgery.
Loss of bone substance, need for augmentation and filling of cavities that must be covered with bone tissue.
Filling of bone cavities in traumatology, dentistry and ophthalmology.
Bone reconstruction and regeneration in traumatology, dentistry and ophthalmology.
Bone reconstruction and regeneration in spinal surgery.
Filler in ocular evisceration and enucleation.
Filler material in the eye socket.
Cranioplasties.
Maxillofacial surgery.
Other clinical indications.
WARNINGS AND PRECAUTIONS

To facilitate bone neoformation, the implanted material must be in direct contact with bone walls with good vascularization and, in certain cases, it is recommended to prepare the patient’s bone tissue with a bur.

In the case of large cavities, a mixture of this biomaterial with autologous bone can improve neoformation.

  • Implantology (dentistry): Experience shows that in areas where bone mass has increased, mechanical load or definitive implant insertion should not be applied until at least 4 to 6 months after insertion of the material.
  • Periodontics (dentistry): Prior to applying the biomaterial, it is necessary to perform a correct treatment of the periodontal lesion by root scaling, curettage and other appropriate procedures.
  • Traumatology: In cases of large fillings, the final mechanical properties in the regenerated area may not be identical to those that would have been obtained with an autologous transplant.

 Any remnants should be discarded and no attempt should be made to resterilize the biomaterial. Do not use after the expiration date.