Other products from "TORNIER, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00846832063253 FHS-010-25-40L HWC Screw, fixation, bone 2 ForeFoot STP
2 00846832066421 DWK403LA25S KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED 2 Aequalis™ PerFORM+
3 00846832064304 FHS-076-31W-12 FHS-076-31W-12 HWC Screw, fixation, bone 2 ForeFoot STP
4 00846832064298 MXM-068C LXH Orthopedic Manual Surgical Instrument 1 ForeFoot STP
5 00846832063802 FHS-010-30F-44 HWC Screw, fixation, bone 2 ForeFoot STP
6 00846832063796 FHS-010-30F-42 HWC Screw, fixation, bone 2 ForeFoot STP
7 00846832063765 FHS-010-30F-36 HWC Screw, fixation, bone 2 ForeFoot STP
8 00846832063703 FHS-010-30F-24 HWC Screw, fixation, bone 2 ForeFoot STP
9 00846832063185 FHS-010-25-26L FHS-010-25-26L HWC Screw, fixation, bone 2 ForeFoot STP
10 00846832063116 FHS-010-25-12L HWC Screw, fixation, bone 2 ForeFoot STP
11 00846832063031 FHS-010-20F-18 HWC Screw, fixation, bone 2 ForeFoot STP
12 00846832085842 MWJ10461 MWJ10461 PHX,KWS shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, SEMI-CONSTRAINE shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED 2 TORNIER PERFORM™ REVERSED
13 00846832085798 DWJ1017702 DWJ1017702 KWS,PHX PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,shoulder prosthes PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,shoulder prosthesis, reverse configuration 2 TORNIER PERFORM™ REVERSED
14 00846832073641 SPS350 SPS350 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
15 00846832073634 SPS348 SPS348 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
16 00846832073627 SPS346 SPS346 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
17 00846832073610 SPS344 SPS344 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
18 00846832073597 SPS340 SPS340 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
19 00846832073580 SPS338 SPS338 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
20 00846832073573 SPS336 SPS336 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
21 00846832073566 SPS334 SPS334 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
22 00846832073559 SPS332 SPS332 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
23 00846832073542 SPS330 SPS330 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
24 00846832073535 SPS328 SPS328 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
25 00846832073511 SPS324 SPS324 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
26 00846832073504 SPS322 SPS322 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
27 00846832073481 SPS318 SPS318 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
28 00846832073474 SPS316 SPS316 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
29 00846832073344 SPS232 SPS232 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
30 00846832073337 SPS230 SPS230 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
31 00846832073320 SPS228 SPS228 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
32 00846832073313 SPS226 SPS226 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
33 00846832073306 SPS224 SPS224 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
34 00846832073283 SPS220 SPS220 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
35 00846832073276 SPS218 SPS218 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
36 00846832073269 SPS216 SPS216 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
37 00846832073252 SPS156 SPS156 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
38 00846832073245 SPS154 SPS154 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
39 00846832073238 SPS152 SPS152 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
40 00846832073221 SPS150 SPS150 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
41 00846832073214 SPS148 SPS148 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
42 00846832073191 SPS144 SPS144 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
43 00846832073184 SPS142 SPS142 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
44 00846832073177 SPS140 SPS140 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
45 00846832073153 SPS136 SPS136 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
46 00846832073146 SPS134 SPS134 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
47 00846832073122 SPS130 SPS130 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
48 00846832073115 SPS128 SPS128 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
49 00846832073108 SPS126 SPS126 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
50 00846832073092 SPS124 SPS124 HWC Screw, fixation, bone 2 ORTHOLOC™ SPS
Other products with the same Product Codes "KWT, KWS, HSD"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 28031497000408 SPS0121 Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder 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 Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, 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 Shoulder 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.). InterSpace Shoulder TECRES SPA
2 28031497000408 SPS0121 Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder 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 Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, 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 Shoulder 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.). InterSpace Shoulder TECRES SPA
3 28031497000392 SPS0021 Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder 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 Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, 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 Shoulder 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.). InterSpace Shoulder TECRES SPA
4 28031497000392 SPS0021 Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder 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 Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, 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 Shoulder 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.). InterSpace Shoulder TECRES SPA
5 10889024287898 01.04255.000 01.04255.000 Anatomical Shoulder™ Bigliani/Flatow® ZIMMER GMBH
6 10889024287898 01.04255.000 01.04255.000 Anatomical Shoulder™ Bigliani/Flatow® ZIMMER GMBH
7 10889024287898 01.04255.000 01.04255.000 Anatomical Shoulder™ Bigliani/Flatow® ZIMMER GMBH
8 10886982241658 5624-8/20XL 5624820XL COCR HUMERAL STEM CEMENTED SIZE 8/200MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
9 10886982241658 5624-8/20XL 5624820XL COCR HUMERAL STEM CEMENTED SIZE 8/200MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
10 10886982241641 5624-8/16L 5624816L COCR HUMERAL STEM CEMENTED SIZE 8/160MM LONG-STERILE NA SYNTHES (U.S.A.) LP
11 10886982241641 5624-8/16L 5624816L COCR HUMERAL STEM CEMENTED SIZE 8/160MM LONG-STERILE NA SYNTHES (U.S.A.) LP
12 10886982241634 5624-8/12 5624812 COCR HUMERAL STEM CEMENTED SIZE 8/120MM-STERILE NA SYNTHES (U.S.A.) LP
13 10886982241634 5624-8/12 5624812 COCR HUMERAL STEM CEMENTED SIZE 8/120MM-STERILE NA SYNTHES (U.S.A.) LP
14 10886982241627 5624-6/19XL 5624619XL COCR HUMERAL STEM CEMENTED SIZE 6/195MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
15 10886982241627 5624-6/19XL 5624619XL COCR HUMERAL STEM CEMENTED SIZE 6/195MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
16 10886982241610 5624-6/15L 5624615L COCR HUMERAL STEM CEMENTED SIZE 6/155MM LONG-STERILE NA SYNTHES (U.S.A.) LP
17 10886982241610 5624-6/15L 5624615L COCR HUMERAL STEM CEMENTED SIZE 6/155MM LONG-STERILE NA SYNTHES (U.S.A.) LP
18 10886982241603 5624-6/11 5624611 COCR HUMERAL STEM CEMENTED SIZE 6/115MM-STERILE NA SYNTHES (U.S.A.) LP
19 10886982241603 5624-6/11 5624611 COCR HUMERAL STEM CEMENTED SIZE 6/115MM-STERILE NA SYNTHES (U.S.A.) LP
20 10886982241597 5624-14/21XL 56241421XL COCR HUMERAL STEM CEMENTED SIZE 14/215MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
21 10886982241597 5624-14/21XL 56241421XL COCR HUMERAL STEM CEMENTED SIZE 14/215MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
22 10886982241580 5624-14/17L 56241417L COCR HUMERAL STEM CEMENTED SIZE 14/175MM LONG-STERILE NA SYNTHES (U.S.A.) LP
23 10886982241580 5624-14/17L 56241417L COCR HUMERAL STEM CEMENTED SIZE 14/175MM LONG-STERILE NA SYNTHES (U.S.A.) LP
24 10886982241573 5624-14/13 56241413 COCR HUMERAL STEM CEMENTED SIZE 14/135MM-STERILE NA SYNTHES (U.S.A.) LP
25 10886982241573 5624-14/13 56241413 COCR HUMERAL STEM CEMENTED SIZE 14/135MM-STERILE NA SYNTHES (U.S.A.) LP
26 10886982241566 5624-12/21XL 56241221XL COCR HUMERAL STEM CEMENTED SIZE 12/210MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
27 10886982241566 5624-12/21XL 56241221XL COCR HUMERAL STEM CEMENTED SIZE 12/210MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
28 10886982241559 5624-12/17L 56241217L COCR HUMERAL STEM CEMENTED SIZE 12/170MM LONG-STERILE NA SYNTHES (U.S.A.) LP
29 10886982241559 5624-12/17L 56241217L COCR HUMERAL STEM CEMENTED SIZE 12/170MM LONG-STERILE NA SYNTHES (U.S.A.) LP
30 10886982241542 5624-12/13 56241213 COCR HUMERAL STEM CEMENTED SIZE 12/130MM-STERILE NA SYNTHES (U.S.A.) LP
31 10886982241542 5624-12/13 56241213 COCR HUMERAL STEM CEMENTED SIZE 12/130MM-STERILE NA SYNTHES (U.S.A.) LP
32 10886982241535 5624-10/20XL 56241020XL COCR HUMERAL STEM CEMENTED SIZE 10/205MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
33 10886982241535 5624-10/20XL 56241020XL COCR HUMERAL STEM CEMENTED SIZE 10/205MM XLONG-STERILE NA SYNTHES (U.S.A.) LP
34 10886982241528 5624-10/16L 56241016L COCR HUMERAL STEM CEMENTED SIZE 10/165MM LONG-STERILE NA SYNTHES (U.S.A.) LP
35 10886982241528 5624-10/16L 56241016L COCR HUMERAL STEM CEMENTED SIZE 10/165MM LONG-STERILE NA SYNTHES (U.S.A.) LP
36 10886982241511 5624-10/12 56241012 COCR HUMERAL STEM CEMENTED SIZE 10/125MM-STERILE NA SYNTHES (U.S.A.) LP
37 10886982241511 5624-10/12 56241012 COCR HUMERAL STEM CEMENTED SIZE 10/125MM-STERILE NA SYNTHES (U.S.A.) LP
38 10886982241467 5540-8/12 5540812 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 8/120MM-STERILE NA SYNTHES (U.S.A.) LP
39 10886982241467 5540-8/12 5540812 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 8/120MM-STERILE NA SYNTHES (U.S.A.) LP
40 10886982241450 5540-6/11 5540611 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 6/115MM-STERILE NA SYNTHES (U.S.A.) LP
41 10886982241450 5540-6/11 5540611 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 6/115MM-STERILE NA SYNTHES (U.S.A.) LP
42 10886982241443 5540-14/13 55401413 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 14/135MM-STER NA SYNTHES (U.S.A.) LP
43 10886982241443 5540-14/13 55401413 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 14/135MM-STER NA SYNTHES (U.S.A.) LP
44 10886982241436 5540-12/13 55401213 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 12/130MM-STER NA SYNTHES (U.S.A.) LP
45 10886982241436 5540-12/13 55401213 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 12/130MM-STER NA SYNTHES (U.S.A.) LP
46 10886982241429 5540-10/12 55401012 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 10/125MM-STER NA SYNTHES (U.S.A.) LP
47 10886982241429 5540-10/12 55401012 TI HUMERAL STEM HA COATED PRESS-FIT SIZE 10/125MM-STER NA SYNTHES (U.S.A.) LP
48 10886982241405 5537-8/12 5537812 TI HUMERAL STEM PRESS-FIT SIZE 8/120MM-STERILE NA SYNTHES (U.S.A.) LP
49 10886982241405 5537-8/12 5537812 TI HUMERAL STEM PRESS-FIT SIZE 8/120MM-STERILE NA SYNTHES (U.S.A.) LP
50 10886982241399 5537-6/11 5537611 TI HUMERAL STEM PRESS-FIT SIZE 6/115MM-STERILE NA SYNTHES (U.S.A.) LP