# K140643: Gryphon BR Anchor W/Proknot Technology,Gryphon Peek Anchor W/ Proknot Technology

- Pathway: 510(k) (Traditional)
- Applicant: Depuy Mitek, A Johnson and Johnson Company
- Decided: Jul 8, 2014 after 118 days
- Product code: MAI (Fastener, Fixation, Biodegradable, Soft Tissue)
- 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: 12 generations back to K971358 (1997). 65 ancestors in all.
No later device cites it as a predicate yet.
0 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132241: Gryphon BR Anchor W/ Proknot Technology, Gryphon BR Anchor W/ Proknot Technology - Hip, Gryphon Peek Anchor W/ Proknot T, Depuy Mitek, A Johnson & Johnson Company (2013) Summary page 1.
- K100012: Gryphon T BR DS Anchor W/Orthocord, Gryphon T BR Anchor W /Orthocord, Gryphon P BR DS Anchor W/Orthocord, Gryphon P BR a, Depuy Mitek, A Johnson & Johnson Company (2010) Summary page 1.
- K090124: Gryphon P BR DS Anchor W/Orthocord,Gryphon P BR Anchor W/Orthocord, Model 210813,210814, Depuy Mitek, A Johnson & Johnson Company (2009) Summary page 1.
- K103712: Gryphon Peek DS Anchor W/ Orthocord, Gryphon Peek Anchor W/ Orthocord, Depuy Mitek, A Johnson & Johnson Company (2011) Summary page 1.

## Indications for use
Gryphon Anchor w/ProKnot Technology is indicated for followings. Shoulder: Bankart Repair, SLAP Lesion Repair, Capsular Shift or Capsulolabml Reconstruction Hip: Capsular Repair. Acetabular Labral Repair

Source page: https://510kreport.com/device/K140643
Methodology: https://510kreport.com/methodology