# K960859: Medpor Ocular Peg System and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Porex Technologies Corp. of Georgia
- Decided: May 29, 1996 after 89 days
- Product code: HPZ (Implant, Eye Sphere)
- Device class: 2
- Regulation: 21 CFR 886.3320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

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

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) The ocular pegging system offered in conjunction with the porous hydroxyapatite sphere implant distributed by Integrated Orbita Implants: named in the summary without a submission number
- (no number) MEDPOR® Ocular Screw and Accessories: named in the summary without a submission number

## Most influential descendants
- K040851: Medpor Attractor Magnetic Coupling System (2004), 0 descendants of its own
- K974203: Perry-Kolberg (PK) Titanium Motility/Support System (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K960859
Methodology: https://510kreport.com/methodology