# K000080: Asnis Iii Cannulated Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Osteonics Corp.
- Decided: Apr 3, 2000 after 83 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
916 later devices descend from it; 21 cite it directly.
1 of 917 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051296: Sijf Cannulated Screw System (2005), 836 descendants of its own
- K060736: Smith & Nephew 6.5MM and 8.0MM Cannulated Screws (2006), 531 descendants of its own
- K090675: Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories (2009), 487 descendants of its own
- K102907: Simmetry Sacroiliac Joint Fusion System (2010), 245 descendants of its own
- K110512: Simmetry Sacroiliac Joint Fusion System (2011), 241 descendants of its own

## Recalls of this device
- Jul 8, 2013 · Class II · Z-2099-2013: Stryker received a report that the length of the cannulated screw asnis III, article # 604640 Lot R11482, was incorrect.

Source page: https://510kreport.com/device/K000080
Methodology: https://510kreport.com/methodology