# K001598: Biobar, Implantable Biodegradable Collagen Membrane for Guided Bone Regeneration

- Pathway: 510(k) (Traditional)
- Applicant: Col-Bar, Ltd.
- Decided: Aug 22, 2000 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
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051267: Gore Resolut Regenerative Material, Gore Resolut XT Regenerative Membrane, Gore Osseoquest Regenerative Membrane (2005), 3 descendants of its own
- K091120: Medpor Contain Implant (2010), 1 descendant of its own
- K132325: Guidor Bioresorbable Matrix Barrier (2013), 0 descendants of its own
- K102184: Medpor Contain Can Implant (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K001598
Methodology: https://510kreport.com/methodology