# K951658: Lactosorb Pop Rivet

- Pathway: 510(k) (Traditional)
- Applicant: Poly-Medics,Inc.
- Decided: Jul 25, 1995 after 106 days
- Product code: JDR (Staple, Fixation, Bone)
- 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
No predicates in its family tree.
29 later devices descend from it; 1 cites it directly.
0 of 30 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
- K961585: Surgical Dynamics Pop Rivet (1996), 28 descendants of its own
- K071920: Autosuture Absorbable Tack and Applicator (2007), 26 descendants of its own
- K091900: Absorbatack 5MM Single Use Absorbable Fixation Device (2009), 12 descendants of its own
- K090470: Autosuture Protack; Tacker System; Absorbatack Fixation Devices (2009), 12 descendants of its own
- K093845: Ethicon Securestrap 5MM Absorbable Strap Fixation Device, Model STRAP25 (2010), 11 descendants of its own

Source page: https://510kreport.com/device/K951658
Methodology: https://510kreport.com/methodology