# K130120: Extremity Medical IP Fusion System

- Pathway: 510(k) (Traditional)
- Applicant: Extremity Medical, LLC
- Decided: Apr 11, 2013 after 84 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: 8 generations back to K962823 (1996). 41 ancestors in all.
No later device cites it as a predicate yet.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073674: Bone Fixation Wire (Kirschner Wire), Signal Medical Corp. (2008) Summary page 1.
- K111419: Osteomed Hand Fusion System, Osteomed LP (2011) Summary page 1.
- K121417: XMCP, Hallux, Tarsx, Extremity Medical Screw System, Extremity Medical, LLC (2012) Summary page 1.

## Indications for use
The Extremity Medical IF Fusion System is intended for reduction and internal fixation of arthrodesis of the interphalangeal joints of the hand.

Source page: https://510kreport.com/device/K130120
Methodology: https://510kreport.com/methodology