# K142339: HEMASORB Resorbable Hemostatic Bone Putty

- Pathway: 510(k) (Special)
- Applicant: Orthocon, LLC
- Decided: Sep 26, 2014 after 36 days
- Product code: MTJ (Wax, Bone)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K791495 (1979). 26 ancestors in all.
No later device cites it as a predicate yet.
1 of 27 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043260: Orthocon LLC Orthostat Hemostatic Bone Putty, Orthocon, LLC (2005) Summary page 4.
- K111575: Hemasorb Absorbable Bone Hemostat Matrix, Orthocon, Inc. (2012) Summary page 4.
- K140117: Ahbppress Absorbable Hemostatic Bone Putty, Orthocon, Inc. (2014) Summary page 4.

## Indications for use
Orthocon HEMASORBpress Resorbable Hemostatic Bone Putty is indicated for use in the control of bleeding from cut or damaged bone by acting as a mechanical barrier or tamponade. The material may be used during surgical procedures and in treating traumatic injurics. HEMASORBpress Resorbable Hemostatic Bone Putty is also indicated for use in the control of bleeding from bone surfaces in cardiothoracic surgery following sternotomy.

Source page: https://510kreport.com/device/K142339
Methodology: https://510kreport.com/methodology