# K033856: 5.0 Cannulated Drill Pin, 6.0 Cannulated Drill-Pin

- Pathway: 510(k) (Traditional)
- Applicant: Peter Stevens, MD
- Decided: Jan 7, 2005 after 393 days
- Product code: KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
This pediatric surgical implant is designed for the following intended purposes: 1. To engage long bones including the femur, tibia, humerus, radius or ulna and permit the bone(s) to be secured to an external fixator or frame via a locking bolt. 2. Thus to stabilize bone fragments to provide fracture alignment and stability; or 3. Thus to stabilize bones that have been surgically cut in order to correct deformities including angular, rotational or length discrepancy.

Source page: https://510kreport.com/device/K033856
Methodology: https://510kreport.com/methodology