# K091243: Ortholoc Ankle Plating System (Aps)

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Jun 26, 2009 after 59 days
- Product code: HRS (Plate, Fixation, Bone)
- 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.
102 later devices descend from it; 3 cite it directly.
0 of 103 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 no predicate by number.

## Most influential descendants
- K102429: Ortholoc 3DI Ankle Plating System, Ortholoc Bone Screw (2010), 97 descendants of its own
- K112772: Ortholoc (TM) Bone Screws (2011), 68 descendants of its own
- K121425: Ortholoc 3DI Ankle Fusion Plating System (2012), 53 descendants of its own
- K140397: Paralock Plating System / Tuffnek Screw (2014), 31 descendants of its own
- K131093: Ortholoc (R) 3DI Ankle Plating System (2013), 26 descendants of its own

## Indications for use
The ORTHOLOC® Ankle Plating System (APS) is intended for fixation of fractures, osteotomies, and non-unions of the distal tibia and fibula.

Source page: https://510kreport.com/device/K091243
Methodology: https://510kreport.com/methodology