# K101902: J Tac Model JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030

- Pathway: 510(k) (Traditional)
- Applicant: Jeil Medical Corporation
- Decided: Feb 8, 2011 after 215 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
Longest line of descent: 3 generations back to K952167 (1995). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022790: The Autotac System Titanium Tack, BioHorizons Implant Systems, Inc. (2002) Summary page 1.

## Indications for use
The J Tac is intended for use to fixate and stabilize bioresorbable and non-resorbable baffler membranes used for regeneration of tissue in the oral cavity or in dental situations that require membrane use or fixation.

Source page: https://510kreport.com/device/K101902
Methodology: https://510kreport.com/methodology