# K895886: Biopro Hemi-Endo Modular Head for PSL System

- Pathway: 510(k) (Traditional)
- Applicant: Biopro, Inc.
- Decided: Dec 1, 1989 after 57 days
- Product code: KWL (Prosthesis, Hip, Hemi-, Femoral, Metal)
- Device class: 2
- Regulation: 21 CFR 888.3360
- Recalls of this device: 1 (0 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.
0 of 1 device 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.

## Recalls of this device
- Sep 9, 2025 · Class II · Z-0149-2026: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Source page: https://510kreport.com/device/K895886
Methodology: https://510kreport.com/methodology