# K213199: Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker GmbH
- Decided: Jan 11, 2022 after 104 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: 5 generations back to K922322 (1992). 21 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000080: Asnis Iii Cannulated Screw System, Howmedica Osteonics Corp. (2000) Summary page 5.
- K140891: Biomet Cannulated Screw System, Biomet, Inc. (2014) Summary page 5.

## Most influential descendants
- K220319: Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System (2022), 1 descendant of its own
- K233912: ARIX Cannulated Screw System (2024), 0 descendants of its own

## Indications for use
The Asnis® III Cannulated Screw System intended for fracture fixation of small and long bones and of the pelvis. The system is not intended for spinal use. The Asnis® PRO Cannulated Screw System 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/K213199
Methodology: https://510kreport.com/methodology