# K151769: Anchorage 2 CP System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker GmbH
- Decided: Oct 27, 2015 after 119 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: 12 generations back to K962616 (1996). 86 ancestors in all.
No later device cites it as a predicate yet.
0 of 87 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063875: Stryker Foot Plating System, Howmedica Osteonics Corp. (2007) Summary page 4.
- K141992: Variax 2 System, Stryker Trauma AG (2014) Summary page 4.

## Indications for use
The Stryker Anchorage 2 CP System is intended for use in internal fixation, reconstruction and treatment of fractures in the foot and ankle in adult and adolescent (12-21 years) patients. Indications include: Replantation Joint fusions Corrective osteotomies Osteopenic bone

Source page: https://510kreport.com/device/K151769
Methodology: https://510kreport.com/methodology