# K170214: Additive Orthopaedics Locking Lattice Plate

- Pathway: 510(k) (Traditional)
- Applicant: Additive Orthopaedics, LLC
- Decided: Apr 13, 2017 after 79 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
Longest line of descent: 13 generations back to K954385 (1996). 206 ancestors in all.
8 later devices descend from it; 2 cite it directly.
0 of 215 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131061: Restore Bunion Correction System, Nextremity Solutions (2013) Summary page 4.
- K140397: Paralock Plating System / Tuffnek Screw, Paragon 28 (2014) Summary page 4.

## Most influential descendants
- K183011: Additive Orthopaedics Patient Specific 3D Locking Lattice Plates (2019), 5 descendants of its own
- K193614: FINE Osteotomy around the knee (2020), 4 descendants of its own
- K211646: FINE Osteotomy (2021), 3 descendants of its own
- K231314: Fine Osteotomy™ (2023), 2 descendants of its own
- K240066: Fine Osteotomy™ (2024), 1 descendant of its own

## Indications for use
The Additive Orthopaedics Locking Lattice Plate is indicated for alignment, stabilization and fusion of fractures, osteotomies and arthrodesis of small bones such as the foot and ankle.

Source page: https://510kreport.com/device/K170214
Methodology: https://510kreport.com/methodology