# K061384: Lorenz Pectus Support Bar, Titanium; Lorenz Pectus Support Bar Stabilizer, Titanium

- Pathway: 510(k) (Special)
- Applicant: Walter Lorenz Surgical, Inc.
- Decided: Jun 6, 2006 after 19 days
- Product code: HRS (Plate, Fixation, Bone)
- 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: 2 generations back to K972420 (1997). 2 ancestors in all.
41 later devices descend from it; 5 cite it directly.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981789: Lorenz Pectus Support Bar Stabilizer, Walter Lorenz Surgical, Inc. (1998) Summary page 1.
- K972420: Lorenz Pectus Support Bar, Walter Lorenz Surgical, Inc. (1997) Summary page 1.

## Most influential descendants
- K073556: Medxpert P.E.S. (Pectus Exacvatum System), Medxpert Stratos (2008), 32 descendants of its own
- K133616: Matrixrib Fixation System (2014), 26 descendants of its own
- K142823: Biomet Microfixation Thoracic Fixation System (2015), 23 descendants of its own
- K151173: Biomet Microfixation RibFix Blu Thoracic Fixation System (2015), 13 descendants of its own
- K152253: Biomet Microfixation RibFix Blu Thoracic Fixation System (2016), 11 descendants of its own

## Indications for use
This device is intended for use in surgical procedures to repair Pectus Excavatum and other chest wall deformities.

Source page: https://510kreport.com/device/K061384
Methodology: https://510kreport.com/methodology