# K071476: Synthes (Usa) 2ND Generation Pelvic C-Clamp

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Aug 24, 2007 after 87 days
- Product code: JEC (Component, Traction, Invasive)
- 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.
No later device cites it as a predicate yet.
0 of 1 device 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 (USA) Pelvic C-Clamp: named in the summary without a submission number

## Indications for use
The Synthes (USA) 2nd Generation Pelvic C-Clamp is intended for emergency stabilization of sacrum fractures or disruptions of the sacroiliac joint with associated circulatory instability.

Source page: https://510kreport.com/device/K071476
Methodology: https://510kreport.com/methodology