# K880402: Codman Surgical Pattie

- Pathway: 510(k) (Traditional)
- Applicant: Codman & Shurtleff, Inc.
- Decided: Mar 2, 1988 after 33 days
- Product code: HBA (Neurosurgical Paddie)
- Device class: 2
- Regulation: 21 CFR 882.4700
- Recalls of this device: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have 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.

## Most influential descendants
- K031008: Aesculap Neuro Patties, Neurosorb 4, 6, and 75 (Green & White) (2003), 1 descendant of its own
- K193346: Codman Surgical Patties & Strips (2020), 0 descendants of its own
- K062406: Aesculap Neuro Patties (2006), 0 descendants of its own

## Recalls of this device
- Jul 16, 2010 · Not classified · Z-0094-2011: Surgical Pattie x-ray stripe (radio-opaque marker) became detached
- Jul 16, 2010 · Not classified · Z-0093-2011: Surgical Pattie x-ray stripe (radio-opaque marker) became detached
- Jul 16, 2010 · Not classified · Z-0095-2011: Surgical Pattie x-ray stripe (radio-opaque marker) may become detached

Source page: https://510kreport.com/device/K880402
Methodology: https://510kreport.com/methodology