# K223772: PRO Plating System, Stryker Trauma Pelvic Set (Matta)

- Pathway: 510(k) (Traditional)
- Applicant: Stryker GmbH
- Decided: Apr 7, 2023 after 112 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 K974908 (1998). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131132: Pelvis II Implant System, Stryker Trauma AG (2013) Summary page 5.
- K001614: Stryker Trauma Pelvic Set, Howmedica Osteonics Corp. (2000) Summary page 5.
- K072411: Aap Bone Plates and Screw Implants, Aap Implantate AG (2008) Summary page 5.

## Most influential descendants
- K260054: I.T.S. PRS Phoenix II (2026), 0 descendants of its own

## Indications for use
The PRO Plating System is indicated for: * Fractures, non-unions, deformities and malunions of the pelvic ring and acetabulum » Sacroiliac joint dislocations The Stryker Trauma Pelvic Set (Matta) is indicated for: * Fractures of the acetabulum, sacrum, illium, and entire pelvic ring; * Revision surgery of pseudarthrosis, non-unions and mal-unions; » Osteonomies; * Arthrodeses; » Sacroilic joint dislocations; » Symphysis pubis disruptions

Source page: https://510kreport.com/device/K223772
Methodology: https://510kreport.com/methodology