# K102352: Evolve Eps Ortholoc

- Pathway: 510(k) (Special)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Dec 2, 2010 after 105 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: 1 generation back to K100146 (2010). 1 ancestor in all.
102 later devices descend from it; 4 cite it directly.
0 of 104 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100146: Evolve Eps Ortholoc, Wrightmedicaltechnologyinc (2010) Summary page 1.

## Most influential descendants
- K113014: Claw II Polyaxial Compression System and Ortholoc 3DSI Locking Screws (2012), 97 descendants of its own
- K121651: Ortholoc 3DI Midfoot/Flatfoot System (2012), 95 descendants of its own
- K140397: Paralock Plating System / Tuffnek Screw (2014), 31 descendants of its own
- K143025: Total Compression Plating System (2014), 24 descendants of its own
- K151442: Total Compression Plating (TCP) System (2015), 23 descendants of its own

## Indications for use
The EVOLVE® BPS ORTHOLOC™ is intended for fixation of fractures, osteotomies and non-unions of the olecranon, humerus, radius and ulna.

Source page: https://510kreport.com/device/K102352
Methodology: https://510kreport.com/methodology