# K223847: CREED™ Cannulated Screws

- Pathway: 510(k) (Special)
- Applicant: Glw, Inc.
- Decided: Jan 25, 2023 after 34 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K792022 (1979). 41 ancestors in all.
No later device cites it as a predicate yet.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200291: CREED™ Cannulated Screws, Glw Medical, Inc. (2020) Summary page 4.

## Indications for use
CREED™ Cannulated Screws are intended to maintain alignment and fixation of bone fractures, comminuted fractures in the presence of appropriate additional immobilization such as rigid fixation implants, cast or brace, nonunions, osteotomies, arthrodesis or bone grafts in the hand, foot, and ankle including distal tibia and fibula. These implants are not intended for spinal use.

Source page: https://510kreport.com/device/K223847
Methodology: https://510kreport.com/methodology