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Hernia fixation devices
The MaxTack™ motorized fixation device provides a push-button firing mechanism, tacks, and an in-line handle design for minimally invasive hernia fixation.
The MaxTack™ device puts powered, stronger mesh fixation†,‡,2 comfortably within your grasp§,||,3–4 — providing you with reliable strength from the first tack to the last.†,5–6
Procedural benefits include:
The MaxTack™ device provides consistently stronger fixation than any other absorbable or permanent tacker, no matter your firing angle.†,‡,¶,**,2 Your minimally invasive hernia procedures can benefit from:
Watch how the design of the MaxTack™ device makes it a game-changer for hernia repair.
The MaxTack™ device delivers easy-to-use,§,||,3,4 innovative hernia repair technology straight out of the box — no assembly required.11 At the pull of a yellow activation tab, two 9V alkaline batteries are ready to power the MaxTack™ device’s push-button firing mechanism, consistently deploying preloaded absorbable tacks while providing you with audible and LED color-coded feedback.||,11,12 An in-line handle design results in greater hand comfort and maneuverability,§,**,3,4 while color-coded tacks (25 violet followed by 5 green) alert you when the tack count is running low.2,13
The MaxTack™ device is single use.
The device may be inserted through a 5 mm cannula, or a larger cannula with the use of a converter, for use in minimally invasive procedures.14
MaxTack™ devices come with a total of 30 absorbable tacks that include two tack colors, 25 violet tacks followed by 5 green tacks, to indicate when the tack count runs low.15,16
Yes, the tacks are absorbable. MaxTack™ device tacks are made of copolymer poly (glycolide-co-L-lactide) (PGLA). This copolymer degrades and is absorbed by hydrolysis as glycolic acid and lactic acid, which are then metabolized by the body.†,17
The absorption profile of PGLA in the first two weeks after initial implantation is minimal, with a significant absorption rate seen in the period from three months to five months after implantation. Following this significant breakdown, the copolymer absorption is essentially completed prior to one year after implantation.†,17
Nonclinical testing demonstrated that a representative polymer tack is MRI-safe. A patient with these tacks can be scanned safely immediately after placement of the tack(s). In nonclinical testing, there is no detectable image artifact caused by the polymer tack.
| Item number | Description | Units per box |
|---|---|---|
|
MAXTACK30 |
6 |
The AbsorbaTack™ fixation device is intended for fixation of prosthetic material to soft tissue in various minimally invasive and open surgical procedures.
The ProTack™ fixation device is used to fix prosthetic material and approximate tissue in various endoscopic surgical specialties such as hernia repair.
The ReliaTack™ fixation device is intended for fixation of prosthetic material to soft tissue in minimally invasive and open surgical hernia repair procedures.
The device is not intended for use where prosthetic material fixation is contraindicated.
TM Third-party brands are trademarks of their respective owners.
Based on benchtop data, not necessarily indicative of human clinical outcomes.
Compared to competitive SorbaFix™*, OptiFix™*, Securestrap™*, and CapSure™* absorbable tackers and Medtronic Absorbatack™ and Reliatack™ absorbable tackers.
Compared to competitive OptiFix™* and Securestrap™* absorbable tackers and Medtronic AbsorbaTack™ absorbable tacker.
Based on surgeon feedback.
Compared to competitive OptiFix™* AT straight-tacker and articulated-tacker and Medtronic ReliaTack™ articulated-tacker.
Compared to competitive Securestrap™* fixation tacker.
Compared to competitive CapSure™* permanent fixation tacker and Medtronic ProTack™ device.
Based on memorandum RE00450435 rev A, MaxTack™ first motorized fixation device memo report. March 2023.
Based on internal report RE00437048, MaxTack™ device fixation strength claims. January 2023.
Based on internal report RE00422041, rev A, Effects of instrument design on body posture with repetitive motions of a lap ventral hernia repair surgeon protocol. October 2022.
Based on internal report RE00422048, Effects of instruments design on body posture with repetitive motions of lap ventral hernia repair surgeon report. August 2022.
Based on internal report RE00435620, MaxTack™ device reliability demonstration report. January 2023.
Based on internal report RE00406203, MaxTack™ device blue overmold trigger button testing and reliability. June 13, 2022.
Based on internal report RE00452165, MaxTack™ device groin indication benchtop testing. March 2023.
Based on internal report RE00453235, MaxTack™ device groin indication preclinical study. March 2023.
Based on memorandum RE00452198 rev A, MaxTack™ device minimizing tissue attachment memo. March 2023.
Based on internal report RE00438086, MaxTack™ device in-vitro mass loss study. December 2022.
Based on internal report RE00336812, MaxTack™ device AVT configuration and technical specification. May 2021.
Based on internal report RE00412158, MaxTack™ device summative usability lab clinician feedback. January 2023.
Based on internal report RE00339412, MaxTack™ tack colors (violet and green) justification. May 2021.
Based on internal report RE00265771, MaxTack™ device shaft length specification. August 2020.
Based on internal report RE00437048, MaxTack™ device fixation strength claims. January 2023.
Based on internal report RE00339412 MaxTack™ tack colors (violet and green) justification. May 2021.
Based on internal report RE00438086, MaxTack™ device in-vitro mass loss study. December 2022.