# K083447: Memometal Anchorage Bone Plate System, Models PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50

- Pathway: 510(k) (Traditional)
- Applicant: Memometal Technologies
- Decided: Feb 6, 2009 after 77 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: 2 generations back to K022325 (2002). 2 ancestors in all.
92 later devices descend from it; 10 cite it directly.
0 of 95 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061808: Darco Locking Bone Plate System, Darco International, Inc. (2006) Summary page 1.

## Most influential descendants
- K131722: I.T.S. Extremity Fixation Systems (2013), 24 descendants of its own
- K132594: Crosscheck Plating System (2013), 23 descendants of its own
- K152974: ORTHOLOC® 3Di Foot Plating Reconstruction System (2015), 22 descendants of its own
- K163293: Colink™ Plating System (2017), 21 descendants of its own
- K172300: CoLink View Plating System (2017), 16 descendants of its own

## Indications for use
The ANCHORAGE® Bone Plate System is indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion, and reconstruction of small bones of the hand, feet, wrist and ankles, fingers and toes. The system may be used in both adults and pediatric patients.

Source page: https://510kreport.com/device/K083447
Methodology: https://510kreport.com/methodology