# K050754: Precimed Cannulated Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Precimed, Inc.
- Decided: May 18, 2005 after 56 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
No predicates in its family tree.
73 later devices descend from it; 2 cite it directly.
0 of 74 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) Cannulated Screw System (S &N Richards): named in the summary without a submission number
- (no number) Cannulated Screw System (Synthes): named in the summary without a submission number

## Most influential descendants
- K073344: Orthopediatrics Plating System (2008), 66 descendants of its own
- K081407: Orthopediatrics Pediplates System (2008), 65 descendants of its own
- K083286: Orthopediatrics Pediloc Locking Plate System (2009), 60 descendants of its own
- K120689: Synthes 3.5 MM VA-LCP Proximal Tibia Plate System (2012), 28 descendants of its own
- K090666: Pediplates (2009), 15 descendants of its own

## Indications for use
The Precimed Cannulated Screw System is indicated for use in the treatment of bone fractures, such as fractures of the tarsals and metatarsals, and for metatarsal and phalangeal osteotomies and arthrodeses.

Source page: https://510kreport.com/device/K050754
Methodology: https://510kreport.com/methodology