# K200113: LINK TrabecuLink Tibial Cones

- Pathway: 510(k) (Traditional)
- Applicant: Waldemar Link GmbH & Co. KG
- Decided: Mar 18, 2020 after 61 days
- Product code: MBH (Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3565
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K982302 (1998). 17 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102896: Trabecular Metal Tibial Cone Augments, Zimmer Trabecular Metal Technology (2010) Summary page 4.
- K153595: Optetrak Logic Metaphyseal Cones, Exactech, Inc. (2016) Summary page 4.

## Most influential descendants
- K201364: LINK TrabecuLink Femoral Cones (2020), 0 descendants of its own

## Indications for use
The LINK® TrabecuLink® Tibial Cones are indicated for patients with severe joint diseases with limitation of mobility due to degenerative, rheumatoid or post-traumatic arthrosis or arthritis and joint fractures which disallow an osteosynthetic reconstruction. The LINK® TrabecuLink® Tibial Cones are indicated for the following conditions: » Surgeries which require implantation of a total knee endoprosthesis after severe degeneration or bone loss, traumata or other pathologies. The device is intended for uncemented use.

Source page: https://510kreport.com/device/K200113
Methodology: https://510kreport.com/methodology