# K010783: 2.0/2.4 Cannulated Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Osteomed Corp.
- Decided: May 30, 2001 after 76 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
No predicates in its family tree.
484 later devices descend from it; 4 cite it directly.
0 of 485 devices in its family (counting itself) have 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
- K062863: Osteomed Extended 2.0/2.4CANNULATED Screw System (2006), 310 descendants of its own
- K103705: Low Profile Screws (2011), 219 descendants of its own
- K051309: Roi Fusion Rods & Plates (2005), 145 descendants of its own
- K080398: SI Joint Fusion System (2008), 144 descendants of its own
- K110838: Ifuse Implant System (2011), 143 descendants of its own

Source page: https://510kreport.com/device/K010783
Methodology: https://510kreport.com/methodology