• PerFuse Handle
• PerFuse Strike Cap
• PerFuse Slide Hammer
• PerFuse Slide Hammer Adapter
• Instrument Case
Intended for Healthcare Professionals
PerFuse™ Percutaneous Decompression System
Biologically Assisted Core Decompression
PerFuse Percutaneous Decompression Instrument is designed to access the femoral or humeral head for core decompression. The system is intended to be used for the delivery of bone graft material to an orthopedic site. It facilitates mixing and pre-mixing of bone graft material with I.V. fluids blood, plasma, bone marrow, or other specified blood components deemed necessary by the clinical use requirements.
Core Decompression is a surgical technique to treat avascular necrosis involving drilling one or more channels into the dead bone (necrotic lesion). Creating a channel into the necrotic lesion is intended to relieve intraosseous pressure within the bone and provide a channel to restore blood flow to the diseased bone.1-2
Procedures
- Treatment Avascular Necrosis (AVN)
Philosophies
- Early Intervention
Application
- Multiple
System Features
The PerFuse system offers flexibility and is easy to use, allowing
orthopaedic surgeons to perform a minimally invasive core
decompression in multiple applications.
Specifications
Benefits
Post-op Flexibility
- The PerFuse cannula creates a 6 mm hole, which offers post-op flexibility for physician
Simple Ease of Use
- PerFuse offers two options in length (Large (295 mm) and Small (161 mm), the disposable components are always sharp and loaner program lowers facility initial investment
Multiple Application Options
- Disposable tamp allows for multiple Intra-operative bone graft options
Eliminate Heat from Power Equipment
- Drill-less technique eliminates heat generated by power equipment
Education
Literature
Videos
PerFuse Percutaneous Decompression System Animation
Watch animation
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Additional Information
Related Products
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Tailored resources for your patients.
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This material is intended for health care professionals. Distribution to any other recipient is prohibited.
For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert or contact your local representative; search this website for additional product information. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please visit labeling.zimmerbiomet.com or call 1-800-348-2759, press 4 for 411 Technical Support.
