# K983814: Gotfried Percutaneous Compression Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Efratgo, Ltd. HI Tech Bio-Surgical
- Decided: Jan 14, 1999 after 78 days
- Product code: JDO (Device, Fixation, Proximal Femoral, Implant)
- 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: 1 generation back to K954555 (1996). 2 ancestors in all.
71 later devices descend from it; 3 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)
- K970097: Proximal Femoral Nail (PFN) System, Synthes (Usa) (1997) Summary page 2.
- K954555: Versa-FX Femoral Fixation System, Zimmer, Inc. (1996) Summary page 2.

## Most influential descendants
- K080434: Intertan CHS Locking Plate System Prox Fem Plates/Screw (2008), 35 descendants of its own
- K090656: Intertan CHS Limited Collapse Set Screw (2009), 34 descendants of its own
- K123055: Smith & Nephew, Inc Screw and Plate System Instrumentation (2013), 33 descendants of its own
- K140814: Evos Mini-Fragment Plating System (2014), 32 descendants of its own
- K031401: Fixion Dynamic Hip Screw System (Fixion DHS) (2003), 32 descendants of its own

## Indications for use
The GOTFRIED PC.C.P is intended to treat stable and unstable intertrochanteric, pertrochanteric, and base of neck hip fractures.

Source page: https://510kreport.com/device/K983814
Methodology: https://510kreport.com/methodology