# K102184: Medpor Contain Can Implant

- Pathway: 510(k) (Traditional)
- Applicant: Porex Surgical, Inc.
- Decided: Jan 7, 2011 after 158 days
- Product code: NPK (Barrier, Synthetic, Intraoral)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K922627 (1994). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091120: Medpor Contain Implant, Porex Surgical, Inc. (2010) Summary page 1.

## Indications for use
The MEDPOR CONTAIN CAN Implant is intended to stabilize, support and provide space maintenance for bone graft materials in the maxilla, mandible and zygoma.

Source page: https://510kreport.com/device/K102184
Methodology: https://510kreport.com/methodology