# K130590: Aap Cannulated Screw 2.0

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Apr 22, 2013 after 46 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K962823 (1996). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071092: Asnis Micro Cannulated Screw, Howmedica Osteonics Corp. (2007) Summary page 1.

## Indications for use
The aap Cannulated Screw 2.0 is intended for fracture fixation of small and long bones and of the pelvis. The system is not intended for spinal use.

Source page: https://510kreport.com/device/K130590
Methodology: https://510kreport.com/methodology