# K183011: Additive Orthopaedics Patient Specific 3D Locking Lattice Plates

- Pathway: 510(k) (Traditional)
- Applicant: Additive Orthopaedics
- Decided: Jan 10, 2019 after 71 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: 14 generations back to K954385 (1996). 271 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 277 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170214: Additive Orthopaedics Locking Lattice Plate, Additive Orthopaedics, LLC (2017) Summary page 4.
- K162674: BioPro Foot Plating Systems, Biopro, Inc. (2017) Summary page 4.

## Most influential descendants
- 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
- K240703: Fine Osteotomy™ (2024), 0 descendants of its own

## Indications for use
The Additive Orthopaedics Patient Specific 3D Printed Locking Lattice Plate is indicated for alignment, stabilization and fusion of fractures, osteotomies and arthrodesis of small bones such as the foot and ankle. It is a patient specific device.

Source page: https://510kreport.com/device/K183011
Methodology: https://510kreport.com/methodology