# K982927: Quick Tap Self Drilling Screw

- Pathway: 510(k) (Special)
- Applicant: Kinamed, Inc.
- Decided: Sep 8, 1998 after 19 days
- Product code: DZL (Screw, Fixation, Intraosseous)
- Device class: 2
- Regulation: 21 CFR 872.4880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K122049: Neuropro Low Profile Cranial Plating System (2013), 0 descendants of its own

## Indications for use
The Kinamed NeuroPro™ , Quick Tap™ Self Drilling Screws are indicated for use in conjunction with bone plates and mesh implants of the parent NeuroPro System in internal fixation of fractures and osteotomies of the craniofacial skeleton including fixation of cranial bone flap osteotomies as well as for reconstruction of bony defects and deficits of the craniofacial skeleton. The Kinamed NeuroPro™ , Quick Tap™ Self Drilling Screws are not indicated for use in the spine.

Source page: https://510kreport.com/device/K982927
Methodology: https://510kreport.com/methodology