# K073336: Codman Craniotomy Kit, Models 26-1229, 26-1230, 26-1231

- Pathway: 510(k) (Special)
- Applicant: Codman & Shurtleff, Inc.
- Decided: Jan 4, 2008 after 37 days
- Product code: HBF (Drills, Burrs, Trephines & Accessories (Compound, Powered))
- Device class: 2
- Regulation: 21 CFR 882.4305
- Recalls of this device: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
1 of 1 device in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Apr 11, 2025 · Class I · Z-1717-2025: Inadequate weld that can potentially cause the product to disassemble.

Source page: https://510kreport.com/device/K073336
Methodology: https://510kreport.com/methodology