# K983754: Standard Chin

- Pathway: 510(k) (Special)
- Applicant: Surgical Technology Laboratories, Inc.
- Decided: Nov 20, 1998 after 29 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.
2 later devices descend from it; 1 cites 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K091011: Pureform Eptfe Facial Implants (Nasal, Chin, Maler) (2009), 1 descendant of its own
- K201153: Tisuthes e-PTFE Surgical Patch (2023), 0 descendants of its own

## Indications for use
Surgical Technology Laboratories, Inc. Standard Chin implants are intended to be used to augment or reconstruct the antenior of the mandible for cosmetic or reconstructive surgery.

Source page: https://510kreport.com/device/K983754
Methodology: https://510kreport.com/methodology