Powerbone Interference Screw
Compression
Information
Implants are supplied sterile and are CE marked. Class III Medical Device according to 93/42/EC medical device directive. Biocompatibility tests (in vitro and in vivo), biodegradation tests, bioburden, and stylerity were applied to the products.
Implants are used for temporary fixation of bone.
Patellar tendon bone and soft tissue grafts in the anterior
Cross ligament and posterior cruciate ligament
Reconstructions.
For user guides and surgical technical documents, please contact.