Ronda Medical
AMES Medical

OsteoSinter® EVANS and COTTON — Porous titanium wedge implants

OsteoSinter® porous titanium wedge implants for the Evans and Cotton osteotomies — correction of foot deformities (acquired flatfoot) with rapid osseointegration, no bone graft, and no supplementary fixation with plates or screws.

OsteoSinter® EVANS and COTTON — porous titanium wedge and the sterile packaging of the EVANS and COTTON ranges (AMES Medical material)
OsteoSinter® porous titaniumMaterial
88%Osseointegration (2 years)
NoneSupplementary fixation
over 2,000Procedures
Clinical description

OsteoSinter® EVANS and COTTON are implantable porous titanium wedges, developed by AMES Medical for the correction of foot deformities — particularly adult-acquired flatfoot (progressive collapsing foot deformity). The wedges are used as an interposition element in opening-wedge osteotomies, restoring and maintaining correction without the need for a bone graft (autograft or allograft).

The OsteoSinter® material (commercially pure titanium, CPTi, manufactured by powder metallurgy and patented — EU2476065B1) has an interconnected, bio-mimetic porosity that reproduces the structure of trabecular bone. This porosity induces osseointegration of the adjacent bone, and its mechanical behavior, similar to that of trabecular bone, has been validated by the Institute of Biomechanics of Valencia (IBV). The high primary fixation eliminates the need for any supplementary fixation (no plates and/or screws).

The EVANS range comprises 9 sizes (footprints of 18×18, 20×20, and 22×22 mm, in heights of 8, 10, and 12 mm) for lateral column lengthening (Evans osteotomy / calcaneal Z osteotomy). The COTTON range comprises 6 sizes (lengths of 15 and 20 mm, in heights of 4.5, 5.5, and 6.5 mm) for the opening-wedge osteotomy of the medial cuneiform (Cotton osteotomy). Implantation is performed with a single-use instrument set (sizers, grasping forceps, and impactor), reducing operative time to 20–30 minutes, with no in-situ shaping. Since its commercial launch in 2021, more than 2,000 procedures have been performed in over 20 countries.

Indications
  • Correction of adult-acquired flatfoot deformity (progressive collapsing foot deformity).
  • Opening-wedge osteotomies of the foot bones, including additive osteotomies for hallux valgus.
  • Cotton osteotomy — opening of the medial cuneiform (correction of forefoot supination).
  • Lateral column lengthening — Evans osteotomy or calcaneal Z osteotomy.
  • Metatarsal/cuneiform (fusion) arthrodeses.
Key features

OsteoSinter® porous titanium (patented)

Interconnected, bio-mimetic porosity similar to trabecular bone — mechanical behavior validated by IBV Valencia.

Rapid osseointegration

88% complete osseointegration at 2 years (clinical study); approximately 61% colonization at 4 weeks (manufacturer data).

No bone graft

An alternative to autograft/allograft — a simpler, faster, and safer procedure, with no iliac crest harvesting.

No supplementary fixation

High primary fixation in bone — no plates and no screws.

Reduced operative time

20–30 minutes; immediately available, with no prior preparation and no in-situ shaping.

Single-use instrumentation

Dedicated set with sizers, grasping forceps, and impactor — precise and reproducible implantation.

Two complementary ranges

EVANS for lateral column lengthening and COTTON for the medial cuneiform.

Product gallery
OsteoSinter® EVANS and COTTON — porous titanium wedge and the sterile packaging of the EVANS and COTTON ranges (AMES Medical material)
OsteoSinter® EVANS and COTTON — porous titanium wedge and the sterile packaging of the EVANS and COTTON ranges (AMES Medical material)
OsteoSinter® — microscopic comparison between trabecular bone and the porous OsteoSinter® material, with bio-mimetic porosity (AMES Medical material)
OsteoSinter® — microscopic comparison between trabecular bone and the porous OsteoSinter® material, with bio-mimetic porosity (AMES Medical material)
OsteoSinter® EVANS and COTTON — before/after radiographs of the surgical correction of the foot deformity (AMES Medical clinical case)
OsteoSinter® EVANS and COTTON — before/after radiographs of the surgical correction of the foot deformity (AMES Medical clinical case)
Technical specifications
Type
Implantable porous titanium wedges for opening-wedge osteotomies and arthrodeses of the foot
Material
Commercially pure titanium (CPTi), porous OsteoSinter® (patent EU2476065B1), manufactured by powder metallurgy
EVANS range
9 sizes — footprints 18×18 / 20×20 / 22×22 mm; heights 8 / 10 / 12 mm (code P00200–P00208)
COTTON range
6 sizes — lengths 15 / 20 mm; heights 4.5 / 5.5 / 6.5 mm (code P00300–P00305)
Fixation
High primary fixation, no supplementary fixation (no plates or screws)
Device class
IIb (Annex IX, Rule 8, 93/42/EEC); non-active functional implant (NANDO MD 0203; GMDN 61617)
Sterilization / use
Gamma radiation; single-use; minimum service life 15 years
Instrumentation
Single-use OsteoSinter® EVANS and COTTON instrument set (sizers, forceps, impactor) — class IIa
Standards
ISO 14630, ISO 14602, ISO 10993 (implant); ISO 16061, ISO 10993 (instruments)
Clinical evidence

A selection of publications and studies that mention use of the system. Summaries are indicative; for details, consult the original source.

Porous Titanium Wedges Associated With High Rates of Osseointegration and Radiologic Correction in Progressive Collapsing Foot Deformity

Montoya-delaTorre C., Ilabaca M.J., García-Jarabo E., García-Elvira R., Vilà y Rico J., Poggio-Cano D. · Foot & Ankle International, 2025

Multicenter, retrospective radiologic study in patients (18–80 years) with flexible acquired flatfoot due to progressive collapse, treated by Evans and Cotton osteotomies with porous titanium wedges between 2019 and 2021, with 2-year follow-up. Radiologic correction (Meary and Kite angles, calcaneal pitch, talonavicular coverage) and osseointegration (Worth classification) were assessed.

88% of feet (38/43) showed complete osseointegration (grade 4) at 2 years; significant radiologic correction across all parameters (Meary 14.7°, p=0.001).
View source
Certifications & compliance
CE marking (MDD 93/42/EEC) ISO 13485:2016

Would you like information about OsteoSinter® EVANS and COTTON — Porous titanium wedge implants?

The Ronda Medical team provides details about availability, configurations, and technical support.

Contact the team