# K832283: Medpar Surgical Implants

- Pathway: 510(k) (Traditional)
- Applicant: Porex Medical
- Decided: May 10, 1984 after 303 days
- Product code: FWP (Prosthesis, Chin, Internal)
- Device class: 2
- Regulation: 21 CFR 878.3550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
36 later devices descend from it; 2 cite it directly.
0 of 37 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
- K053199: Synthes Patient Specific Cranial/Craniofacial Implant (2005), 34 descendants of its own
- K062570: Patient Contoured Mesh (PCM) (2006), 17 descendants of its own
- K121153: Peek Customized Craial Implant Kit (2012), 13 descendants of its own
- K072707: Patient Contoured Mesh-Peek (PCM-P) (2007), 13 descendants of its own
- K103582: Kelyniam Custom Skull Implant (Csi) (2011), 8 descendants of its own

Source page: https://510kreport.com/device/K832283
Methodology: https://510kreport.com/methodology