Intraosseous device for inserting a cannula into a bone

1. A device for the insertion of a cannula into a bone of a patient, which comprises:

a. an activator assembly for activating the device;

b. a needle assembly which comprises a stylet and cannula;

c. a barrel assembly for containing said stylet and cannula in a loaded state prior to the device activation; and

d. a setting assembly for adjusting a penetration depth of said cannula into the patient's bone;

wherein:

e. said activator assembly comprises a first safety mechanism in a form of a safety catch that prevents activation of the device unless said safety catch is released;

f. said activator assembly comprises a trigger that triggers activation of the device only if pulled toward a proximal direction, while pulling to a distal direction is prevented, thereby eliminating reverse direction activation;

g. the device comprises a second safety mechanism that prevents activation of the device by locking it unless said setting assembly is pushed against a patient's body, thereby causing closure of a gap in the device between a jacket which is located in said barrel assembly and said activator assembly, hence the device becomes ready for activation only when placed properly against the patient's body.

2. A device according to claim 1 , wherein said gap between said barrel assembly and said activator assembly is formed by means of a secondary spring which is located between said two assemblies.

3. A device according to claim 1 , wherein when the device is pushed against the patient's body, but released without triggering, the gap is recreated, and the device becomes locked again.

4. A device according to claim 1 , wherein said needle assembly is maintained in a loaded state within the device by means of a loaded main spring.

5. A device according to claim 1 , wherein said setting assembly automatically separates from a main body of the device together with said needle assembly after activation of the device, and said setting assembly remains on the patient's body to support, stabilize, fix and maintain the cannula in place.

6. A device according to claim 1 , wherein the stylet is removed from the cannula after activation of the device, leaving the cannula penetrated within the bone, thereby producing a channel from the exterior of the patient's body to within the medullary cavity of the bone.

7. A device according to claim 1 , wherein said first safety mechanism is released by means of rotating said first safety mechanism relative to the rest of the device.

8. A device according to claim 1 , wherein said stylet is maintained within said cannula, before activation of the device.

9. A device according to claim 1 , wherein said setting assembly comprises a turning element with a thread, which defines the penetration depth by means of rotation.

10. A device according to claim 1 , wherein said needle assembly is pushed toward the bone upon activation of the device by means of a hammer.

11. A device according to claim 1 , wherein said needle assembly further comprises a first holder, said first holder releases the stylet and cannula after the triggering of the device.

12. A device according to claim 11 , wherein said first holder automatically releases the setting assembly after the triggering of the device and insertion of said stylet and cannula into the bone.

13. A device according to claim 1 , wherein said needle assembly comprises a needle holder that holds the needle aligned in place during the loaded state of the device.

14. A device according to claim 1 , wherein said second safety mechanism allows activation of the device only when positioned essentially perpendicular to a bone surface.

15. A device according to claim 1 , wherein the setting assembly is pre-adjusted to a fixed penetration depth.