# K141219: Juggerloc Bone to Bone Implants/ Bone Instruments/ Bone Implant and Instrument Kits

- Pathway: 510(k) (Traditional)
- Applicant: Biomet Manufacturing Corp
- Decided: Jul 18, 2014 after 67 days
- Product code: HTN (Washer, Bolt Nut)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K792022 (1979). 71 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 73 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130033: Toggleloc Xtender; Toggleloc XL; Implant Kit Toggleloc; Implant Kit Toggleloc BTB, Extended Toggleloc; Toggleloc; BTB to, Biomet Manufacturing Corp (2013) Summary page 1.
- K110145: Biomet Sports Medicine Juggerknot Soft Anchor, Biomet, Inc. (2011) Summary page 1.
- K133275: Mini Tightrope, Arthrex, Inc. (2014) Summary page 1.

## Most influential descendants
- K172620: SyndesMetrics Syndesmosis Repair System (2017), 0 descendants of its own

## Indications for use
The Biomet JuggerLocT" Bone to Bone system is Intended for repair in the foot and ankle Including indications for: Midfoot repair including but not limited to Lisfranc repair, ankle syndlesmosis fixation (syndesmosis disruptions), and as an adjunct In connection with trauma hardware for Weber B and C ankle fractures.

Source page: https://510kreport.com/device/K141219
Methodology: https://510kreport.com/methodology