# K050292: Sharpoint Lukens Bone Wax

- Pathway: 510(k) (Traditional)
- Applicant: Surgical Specialties Corp
- Decided: Mar 9, 2005 after 30 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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) Ethicon, Inc. Bone Wax: named in the summary without a submission number
- (no number) CP Medical, Inc. Bone Wax: named in the summary without a submission number

## Most influential descendants
- K200452: Meril-Bonewax (2023), 0 descendants of its own

## Indications for use
Sharpoint Lukens® bone wax is indicated for use for control of bleeding from bone surface during surgical operations.

Source page: https://510kreport.com/device/K050292
Methodology: https://510kreport.com/methodology