# K172148: Anchorage Bone Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker GmbH
- Decided: Mar 19, 2018 after 245 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: 3 generations back to K022325 (2002). 3 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083447: Memometal Anchorage Bone Plate System, Models PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50, Memometal Technologies (2009). Our reading of the summary gave K083477, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Anchorage Bone Plating System”.

## Most influential descendants
- K202657: Javelin Tailor's Bunion Fixation System (2020), 1 descendant of its own
- K202959: PolyLock Plating System (2020), 1 descendant of its own
- K260291: Vortex5 Tailor's Bunion Correction System (2026), 0 descendants of its own
- K211843: PolyLock Plating System (2022), 0 descendants of its own

## Indications for use
The Anchorage Bone Plating System is indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion, and reconstruction of small bones in the hands, feet, wrists, ankles, fingers, and toes. The system may be used in adults and pediatric patients.

Source page: https://510kreport.com/device/K172148
Methodology: https://510kreport.com/methodology