# K132241: Gryphon BR Anchor W/ Proknot Technology, Gryphon BR Anchor W/ Proknot Technology - Hip, Gryphon Peek Anchor W/ Proknot T

- Pathway: 510(k) (Traditional)
- Applicant: Depuy Mitek, A Johnson & Johnson Company
- Decided: Nov 5, 2013 after 110 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: 11 generations back to K971358 (1997). 64 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121018: Bioraptor 2.9, Bioraptor 2.3 PK, Osteoraptor, & Bioraptor Knotless Suture an, Smith & Nephew, Inc. (2012) Summary page 1.
- K093428: Smith & Nephew Knotless Instability Anchor, Smith & Nephew Endoscopy, Inc. (2009) 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.
- 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.
- K103712: Gryphon Peek DS Anchor W/ Orthocord, Gryphon Peek Anchor W/ Orthocord, Depuy Mitek, A Johnson & Johnson Company (2011) Summary page 1.

## Most influential descendants
- K140643: Gryphon BR Anchor W/Proknot Technology,Gryphon Peek Anchor W/ Proknot Technology (2014), 0 descendants of its own

## Indications for use
GRYPHON ANCHOR wiPROKNOT TECHNOLOGY is indicated for followings. Shoulder: Bankart Repair, SLAP Lesion Repair, Capsular Shift or Capsulolabral Reconstruction Hip: Capsular Repair, Acetabular Labral Repair

Source page: https://510kreport.com/device/K132241
Methodology: https://510kreport.com/methodology