DUAL OFFSET BROACH HANDLE, LEFT, NO TWIST

DUAL OFFSET BROACH HANDLE, RIGHT, NO TWIST

CALCAR PLANER BLADE 1.3"

CALCAR PLANER BLADE 1"

CANAL FINDER, TOOTHED STARTER BROACH

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

Alteon Highly Polished Femoral Stem

EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL

EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL

EXETER MIS HALF MOON FEMORAL CEMENT SEAL

SPECIALTY TRIDENT TRIAL CONTAINMENT SCREW-LONGER

MODULAR POROUS BIOGRIP® COLLAR, 24MM, UNCOATED

MODULAR POROUS BIOGRIP® COLLAR, 28MM, UNCOATED

MODULAR POROUS BIOGRIP® COLLAR, 32MM, UNCOATED

MODULAR POROUS BIOGRIP® COLLAR, 36MM, UNCOATED

MODULAR POROUS BIOGRIP® COLLAR, 40MM, UNCOATED

SEGMENTAL COLLAR STEM, CEMENTED, 9MM X 100MM

SEGMENTAL COLLAR STEM, CEMENTED, 10MM X 100MM

SEGMENTAL COLLAR STEM, CEMENTED, 11MM X 100MM

SEGMENTAL COLLAR STEM, CEMENTED, 13MM X 100MM

SEGMENTAL COLLAR STEM, CEMENTED, 15MM X 100MM

SEGMENTAL COLLAR STEM, CEMENTED, 17MM X 100MM

ELEOS MODULAR COLLAR LOCKING RING

ELEOS MODULAR COLLAR LOCKING RING AND IMPACTOR TIP

Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cementcoated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.).

Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.).

Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.).

Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.).

Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.).

Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.).