# K202680: OsteoMed ExtremiFix Mini & Small Cannulated Screw System

- Pathway: 510(k) (Special)
- Applicant: Osteomed, LLC
- Decided: Oct 15, 2020 after 30 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
Longest line of descent: 6 generations back to K962823 (1996). 15 ancestors in all.
7 later devices descend from it; 3 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063298: Osteomed Headless Cannulated Screw System, Osteomed LP (2007) Summary page 4.

## Most influential descendants
- K210754: Cannulated Fasteners and Nuts (2021), 3 descendants of its own
- K211290: Cannulated Fasteners and Nuts (2021), 2 descendants of its own
- K230744: Acumed Acutrak 3 Headless Compression Screw System (2023), 1 descendant of its own
- K250251: Eleganz Fusion Screw System (Fusion Screw System) (2025), 0 descendants of its own
- K242691: OsteoCentric Technologies Cannulated Fasteners and Nuts (2024), 0 descendants of its own

## Indications for use
The Osteomed ExtremiFix Mini & Small Cannulated Screw System is indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation of bones appropriate for the size of the device. Screws are intended for single use only.

Source page: https://510kreport.com/device/K202680
Methodology: https://510kreport.com/methodology