Engineered Sterile Allograft for Arthrodesis

The AlloAid^® PIP is a sterile, engineered Allograft.

The Allograft is supplied in 2 sizes featuring both straight and 10° angled configurations. The AlloAid^® PIP complies with all FDA, AATB and state regulatory requirements for donor screening, recovery and testing.

Designed with Positioning Ramps to help accurately position the implant and ensure a press-fit.
Sterile aAllograft has conductive properties.
No post-op hardware removal needed.
Available in both straight & 10° angled configurations.

The AlloAid^® PIP Allograft is designed with Positioning Ramps at the joint line to help accurately position the implant and ensure a press-fit and reduce the chance of subsidence. The cross-sectional shape and tapered design resist rotation. Tapered ends help with ease of insertion.

Instrument Kit:

The AlloAid^® PIP Allograft is accompanied by a simple and convenient instrument set that includes bowed-nose Forceps and laser-marked Reamers.

Sterile Disposable Instrument Kit

Ordering Information:

Representation of SAL (Sterility Assurance Level). Designates the occurrence of a living microorganism surviving the sterilization process. SAL of 10^-6 designates that the possibility of finding an unsterile product will be 1 in a million. While other sterilization methods have also been shown to inactivate viruses, they can be detrimental to the biological and physical properties of allograft bone.

CAUTION: Federal law (USA) restricts this device to sale and use by, or on the order of, a physician.

All content contained herein is furnished for informational purposes only. In2Bones does not recommend a particular surgical product or procedure suitable for all patients. Each surgeon must evaluate the appropriateness of a device and corresponding techniques based on medical training, clinical judgment and surgical experience. The proper surgical technique and/or procedure are the responsibility of the medical professional. Indications, contraindications, warnings and precautions are listed in the implant package insert and should be reviewed carefully by the physician and operating room personnel prior to any proposed procedure. Availability of these products might vary from one given country or region to another as a result of specific local regulatory approval or clearance requirements for sale in such country or region.