# K972842: Interpore Inducer Bone Graft Delivery Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Intl.
- Decided: Oct 30, 1997 after 90 days
- Product code: LYC (Bone Grafting Material, Synthetic)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K841201 (1984). 1 ancestor in all.
1 later device descends 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)
- K841201: Porous Hydroxyapatite BG200, Interpore Intl. (1984)
- (no number) Grafton Allogeneic Bone Matrix Syringe: named in the summary without a submission number

## Most influential descendants
- K041344: Open Bore Syringe (2004), 0 descendants of its own

## Indications for use
The Interpore Inducer Bone Graft Delivery Syringe is indicated for the delivery of allograft, autograft or synthetic bone graft material to an orthopaedic surgical site. In addition, it is designed to facilitate pre-mixing of a bone graft material with 1.V. fluids, blood, plasma, bone marrow or other specific blood component(s) as deemed necessary by the clinical use requirements. The Interpore Inducer has a volume of approximately 15 cc.

Source page: https://510kreport.com/device/K972842
Methodology: https://510kreport.com/methodology