# K051296: Sijf Cannulated Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Depuy Spine, Inc.
- Decided: Aug 26, 2005 after 100 days
- Product code: OUR (Sacroiliac Joint Fixation)
- 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: 1 generation back to K903810 (1990). 3 ancestors in all.
836 later devices descend from it; 6 cite it directly.
1 of 840 devices in its family (counting itself) has 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 1.
- K024060: Modification to Asnis Iii Cannulated Screw System, Howmedica Osteonics Corp. (2002) Summary page 1.
- K903810: Ace Cannulated Self Tapping Cancellous Bone Screw, Ace Medical Co. (1990) Summary page 1.

## Most influential descendants
- 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
- K111801: Simmetry (TM) Sacroiliac Joint Fusion System (2011), 240 descendants of its own

## Indications for use
The SIJF Cannulated Screw is intended for fracture fixation of long bones and of the pelvis for such conditions as degenerative sacroiliitis, trauma (fracture and/or dislocation) or tumor, iatrogenic instability and Osteitis Condensans llii. The system is not intended for spinal use.

Source page: https://510kreport.com/device/K051296
Methodology: https://510kreport.com/methodology