# K992239: Pillar Chin Implant

- Pathway: 510(k) (Traditional)
- Applicant: Pillar Surgical, Inc.
- Decided: Nov 22, 1999 after 143 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.
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. The FDA summary names its predicate without a number.
- (no number) Silimed Chin Implants: named in the summary without a submission number

## Indications for use
Each Pillar Chin Implant is indicated for the augmentation or reconstruction of chin deficiencies, whether congenital or acquired by trauma or disease.

Source page: https://510kreport.com/device/K992239
Methodology: https://510kreport.com/methodology