# K014185: Aos Cannulated Bone Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Orthopaedic Solutions, Inc.
- Decided: Feb 13, 2002 after 55 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Smith and Nephew 5.5mm and 7.0mm Titanium and Stainless Steel Cannulated Screws: named in the summary without a submission number
- (no number) Smith and Nephew 6.5mm and 4.0mm Cannulated Screws: named in the summary without a submission number
- (no number) Howmedica Osteonics ASNIS III Cannulated Screw System: named in the summary without a submission number

## Most influential descendants
- K030619: Odi 7.0MM Cannulated Screw System (2003), 0 descendants of its own

## Indications for use
The AOS Cannulated Bone Screw System is intended for fracture fixation of small and long bones and of the pelvis. This system is not intended for spinal use.

Source page: https://510kreport.com/device/K014185
Methodology: https://510kreport.com/methodology