Arthroscopy — ACL suspensory fixation
T-Button®
Adjustable loop UHMWPE suture PEEK button for tibial suspensory fixation. USFDA 510(k) cleared, providing secure, strong and biocompatible graft fixation.
Arthroscopy — ACL suspensory fixation
Adjustable loop UHMWPE suture PEEK button for tibial suspensory fixation. USFDA 510(k) cleared, providing secure, strong and biocompatible graft fixation.
Newtons+ pull-out strength
mm disc head diameter
mm stub diameter
01 — Design features
Seven design decisions behind the button — dimensions, material, loop and fit.
01
Stub diameter 7.5 mm for optimal seating in the bone tunnel; disc head diameter 16 mm ensures effective load distribution.
02
PEEK is an MRI-safe and chemically inert material that minimizes reactions.
03
UHMWPE fibre size 3, offering high strength and durability.
04
A single tendon suffices for a short and thick graft.
05
1300N+ strength for long-term stability.
06
The stub secures the button inside the tunnel; the head rests flush against the tibial cortex with minimal protrusion above the bone surface.
07
One-size-fits-all design simplifies inventory management and suits surgical needs.
02 — Available options
| Variant | Description |
|---|---|
| T-Button (Closed) | Adjustable loop 16 mm × 90 mm — preloaded with 90 mm adjustable loop |
| T-Button (Open) | Open button with loop |
Scientific evidence
Dr. Sunil K. Dash, Dr. Dinesh Mishra and Dr. Harekrushna Sahu
Dr. Neeraj Adkar, Dr. Satwik Thareja, Dr. Ravi A. Kerhalkar and Dr. Prajwal Sadalagi
Dr. Apurve Parameswaran, Dr. Suraj Kumar Choudhary Konka, Dr. Murtuza Ahmed Mohammed, Dr. Krishna Kiran Eachempati and Dr. Sunil Apsingi
04 — Ordering information
| Code | Description |
|---|---|
| S23-1600-K | Adjustable Loop UHMWPE Suture PEEK Open Button — 90 mm |
| S23-1690-K | Adjustable Loop UHMWPE Suture PEEK Close Button — 90 mm |
| Code | Description |
|---|---|
| S25-TB02-A | T-Button dilator |
| S25-TB01-A | Button holder suture tightening post |
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Disclaimer: responsibility for administering products mentioned and interpretation of clinical data provided lies with the registered medical practitioner. For more information about products, please refer to the Instructions for Use (IFU) document. Reference: data on file.

Helysis®