# K173562: Straumann Jason Membrane

- Pathway: 510(k) (Traditional)
- Applicant: Institut Straumann AG
- Decided: Jul 9, 2018 after 234 days
- Product code: NPL (Barrier, Animal Source, Intraoral)
- 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: 6 generations back to K924408 (1995). 9 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141177: Vitala Porcine Derived Collagen Membrane, Osteogenics Biomedical, Inc. (Formerly Obi Biologi (2015) Summary page 4.

## Most influential descendants
- K242817: Jason membrane (2025), 0 descendants of its own
- K223912: InterCollagen® Guide (2023), 0 descendants of its own

## Indications for use
Jason Membrane alone or in combination with suitable augmentation materials (like autogenous bone, allogeneic, xenogeneic or alloplastic bone replacement materials) is indicated for immediate or delayed guided tissue and bone regeneration. in case of surgical bone defects and bone wall defects in the context of sinus floor augmentation and for support of the Schneiderian membrane in the context of maxillary ridge augmentation in the context of maxillary ridge reconstruction for prosthetic treatment in the context of a treatment of fenestration defects in case of periodontal bone defects (one to three-wall defects, class I and II furcation defects) in case of dehiscence defects after apicoectomy, cystectomy, resection of retained teeth and resection of other bone lesions in extraction sockets after tooth extractions in case of immediate or delayed augmentation around implants in extraction sockets

Source page: https://510kreport.com/device/K173562
Methodology: https://510kreport.com/methodology