# K001614: Stryker Trauma Pelvic Set

- Pathway: 510(k) (Traditional)
- Applicant: Howmedica Osteonics Corp.
- Decided: Aug 4, 2000 after 71 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single Component)
- 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
No predicates in its family tree.
12 later devices descend from it; 5 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Synthes Pelvic Implant Set: named in the summary without a submission number

## Most influential descendants
- K063166: I.T.S. Pelvic Reconstruction System (2006), 9 descendants of its own
- K131132: Pelvis II Implant System (2013), 5 descendants of its own
- K122538: Acumed Pelvic Bone Plate System (2012), 4 descendants of its own
- K210935: I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix) (2022), 3 descendants of its own
- K161894: SurgTech Trauma System (2017), 3 descendants of its own

## Indications for use
The Stryker TraumaPelvic Set is indicated for: Fractures of the acetabulum, sacrum, illium., and entire pelvic ring Revision surgery of pseoduarthroses, non-unions and mal-unions Osteonomies Arthrodeses Sacroihc joint dislocations Symphysis pubis disruptures

Source page: https://510kreport.com/device/K001614
Methodology: https://510kreport.com/methodology