# K070169: KLS Martin Quick Disc, Sternal Talon and Sternal Plating - Sterile

- Pathway: 510(k) (Traditional)
- Applicant: KLS Martin L.P.
- Decided: Mar 26, 2007 after 67 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: 8 generations back to K761228 (1976). 81 ancestors in all.
61 later devices descend from it; 6 cite it directly.
0 of 143 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062857: KLS Martin Quick Disc, KLS Martin L.P. (2006) Summary page 2.
- K051165: KLS Martin Sternal Talon, KLS-Martin L.P. (2006) Summary page 2.
- K032413: KLS-Martin Sternal Plating System, KLS-Martin L.P. (2003) Summary page 2.
- K060177: KLS Martin Rigid Fixation  - Sterile, KLS Martin L.P. (2006) Summary page 2.

## Most influential descendants
- K151983: KLS Martin LSS Plating System (2016), 45 descendants of its own
- K202889: Able Medical Devices Valkyrie Thoracic Fixation System (2021), 39 descendants of its own
- K220782: IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System, Transcend™ PEEK Interbody System, Transcend™ NanoTec™ Interbody System, IdentiTi™ ALIF Standalone Interbody System, IdentiTi™ NanoTec™ ALIF Standalone Interbody System, IdentiTi™ Cervical Standalone Interbody System, IdentiTi™ NanoTec™ Cervical Standalone Interbody System (2022), 36 descendants of its own
- K222028: IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System, Transcend™ PEEK Interbody System, Transcend™ NanoTec™ Interbody System, IdentiTi™ ALIF Standalone Interbody System, IdentiTi™ NanoTec™ ALIF Standalone Interbody System (2022), 28 descendants of its own
- K222973: IdentiTi and Transcend Interbody Systems: IndentiTi Cervical Porous Ti Interbody System, IdentiTi NanoTec Cervical Interbody System, Transcend Cervical PEEK Interbody System, Transcend NanoTec Cervical Interbody System, IdentiTi Cervical Standalone Interbody System, IdentiTi NanoTec Cervical Standalone Interbody Sytem (2022), 13 descendants of its own

## Indications for use
To offer KLS Martin Quick Disc, KLS Martin Sternal Talon and KLS Martin Sternal Plating in sterile packaging with the following indications for use: K062857 KLS Martin Quick Disc is intended for use in the reattachment of cranial bone flaps after a craniotomy, covering burr holes, and fixation of cranial fractures. K051165 KLS Martin Sternal Talon and K032413 KLS Martin Sternal Plating System are intended for use in stabilization and fixation of anterior chest wall fractures including sternal fixation subsequent to sternotomy and sternal reconstructive procedures.

Source page: https://510kreport.com/device/K070169
Methodology: https://510kreport.com/methodology