# K062406: Aesculap Neuro Patties

- Pathway: 510(k) (Special)
- Applicant: Aesculap, Inc.
- Decided: Sep 15, 2006 after 29 days
- Product code: HBA (Neurosurgical Paddie)
- Device class: 2
- Regulation: 21 CFR 882.4700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K880402 (1988). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031008: Aesculap Neuro Patties, Neurosorb 4, 6, and 75 (Green & White), Aesculap (2003) Summary page 1.

## Indications for use
Aesculap's Neuro Patties are intended for use during surgery to protect nervous tissue, absorb fluids, or stop bleeding during neurological and other general procedures.

Source page: https://510kreport.com/device/K062406
Methodology: https://510kreport.com/methodology