Other products from "ZIMMER, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024233638 42-5112-004-10 42-5112-004-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
2 00889024233621 42-5112-003-20 42-5112-003-20 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
3 00889024233614 42-5112-003-18 42-5112-003-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
4 00889024233607 42-5112-003-16 42-5112-003-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
5 00889024233591 42-5112-003-14 42-5112-003-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
6 00889024233584 42-5112-003-13 42-5112-003-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
7 00889024233577 42-5112-003-12 42-5112-003-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
8 00889024233560 42-5112-003-11 42-5112-003-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
9 00889024233553 42-5112-003-10 42-5112-003-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
10 00889024233546 42-5112-002-20 42-5112-002-20 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
11 00889024233539 42-5112-002-18 42-5112-002-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
12 00889024233522 42-5112-002-16 42-5112-002-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
13 00889024233515 42-5112-002-14 42-5112-002-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
14 00889024233508 42-5112-002-13 42-5112-002-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
15 00889024233492 42-5112-002-12 42-5112-002-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
16 00889024233485 42-5112-002-11 42-5112-002-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
17 00889024233478 42-5112-002-10 42-5112-002-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
18 00889024233461 42-5112-001-20 42-5112-001-20 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
19 00889024233454 42-5112-001-18 42-5112-001-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
20 00889024233447 42-5112-001-16 42-5112-001-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
21 00889024233430 42-5112-001-14 42-5112-001-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
22 00889024233423 42-5112-001-13 42-5112-001-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
23 00889024233416 42-5112-001-12 42-5112-001-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
24 00889024233409 42-5112-001-11 42-5112-001-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
25 00889024233393 42-5112-001-10 42-5112-001-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
26 00889024233386 42-5110-007-18 42-5110-007-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
27 00889024233379 42-5110-007-16 42-5110-007-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
28 00889024233362 42-5110-007-14 42-5110-007-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
29 00889024233355 42-5110-007-13 42-5110-007-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
30 00889024233348 42-5110-007-12 42-5110-007-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
31 00889024233331 42-5110-007-11 42-5110-007-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
32 00889024233324 42-5110-007-10 42-5110-007-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
33 00889024233317 42-5110-006-18 42-5110-006-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
34 00889024233300 42-5110-006-16 42-5110-006-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
35 00889024233294 42-5110-006-14 42-5110-006-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
36 00889024233287 42-5110-006-13 42-5110-006-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
37 00889024233270 42-5110-006-12 42-5110-006-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
38 00889024233263 42-5110-006-11 42-5110-006-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
39 00889024233256 42-5110-006-10 42-5110-006-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
40 00889024233249 42-5110-005-18 42-5110-005-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
41 00889024233232 42-5110-005-16 42-5110-005-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
42 00889024233225 42-5110-005-14 42-5110-005-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
43 00889024233218 42-5110-005-13 42-5110-005-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
44 00889024233201 42-5110-005-12 42-5110-005-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
45 00889024233195 42-5110-005-11 42-5110-005-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
46 00889024233188 42-5110-005-10 42-5110-005-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
47 00889024233171 42-5110-004-18 42-5110-004-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
48 00889024233164 42-5110-004-16 42-5110-004-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
49 00889024233157 42-5110-004-14 42-5110-004-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
50 00889024233140 42-5110-004-13 42-5110-004-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
Other products with the same Product Codes "HWT, LYS"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00812388031060 FA 0208-01 CTH-615-07 Trial Head, 6M (6mm H x 15mm W x 12.5mm D), G7 M6-C SPINAL KINETICS, INC.
2 00812388031046 FA 0190 CSA-100-07 Stop Assembly, G7 M6-C SPINAL KINETICS, INC.
3 00812388031039 FA 0189 CUH-100-07 Universal Handle Assembly, G7 M6-C SPINAL KINETICS, INC.
4 00812388030285 FA 0191 CIH-100-06 Trial Handle, G6 M6-C SPINAL KINETICS, INC.
5 00812388030278 FA 0192-08 CTH-717L-06 Trial Head, 7LL (7mm H x 17mm W x 16mm D), G6 M6-C SPINAL KINETICS, INC.
6 00812388030261 FA 0192-06 CTH-717-06 Trial Head, 7L (7mm H x 17mm W x 14mm D), G6 M6-C SPINAL KINETICS, INC.
7 00812388030254 FA 0192-04 CTH-715L-06 Trial Head, 7ML (7mm H x 15mm W x 15mm D), G6 M6-C SPINAL KINETICS, INC.
8 00812388030247 FA 0192-02 CTH-715-06 Trial Head, 7M (7mm H x 15mm W x 12.5mm D), G6 M6-C SPINAL KINETICS, INC.
9 00812388030230 FA 0192-07 CTH-617L-06 Trial Head, 6LL (6mm H x 17mm W x 16mm D), G6 M6-C SPINAL KINETICS, INC.
10 00812388030216 FA 0192-03 CTH-615L-06 Trial Head, 6ML (6mm H x 15mm W x 15mm D), G6 M6-C SPINAL KINETICS, INC.
11 00812388030209 FA 0192-01 CTH-615-06 Trial Head, 6M (6mm H x 15mm W x 12.5mm D), G6 M6-C SPINAL KINETICS, INC.
12 00812388030193 FA 0195-02 CFT-200L-06 Footprint Template, L/LL, G6 M6-C SPINAL KINETICS, INC.
13 00812388030186 FA 0195-01 CFT-200M-06 Footprint Template, M/ML, G6 M6-C SPINAL KINETICS, INC.
14 00812258028091 MR2-4090T MR2-4090T Trial Rod Template - for use with the MAGEC® Spinal Bracing and Distraction System MAGEC® Rod Template NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
15 00812258028084 MR2-4070T MR2-4070T Trial Rod Template - for use with the MAGEC® Spinal Bracing and Distraction System MAGEC® Rod Template NUVASIVE SPECIALIZED ORTHOPEDICS, INC.
16 00810933031367 1080-672 1080-672 Cordera Cup Digital Template Cordera Hip System CONFORMIS, INC.
17 00810933031404 1080-673 1080-673 Actera Stem Digital Template Actera hip system CONFORMIS, INC.
18 00810933031398 1080-670 1080-670 Actera Stem Acetate -120% Magnification Template Actera hip system CONFORMIS, INC.
19 00810933031381 1080-669 1080-669 Actera Stem Acetate -115% Magnification Template Actera hip system CONFORMIS, INC.
20 00810933031374 1080-668 1080-668 Actera Stem Acetate -110% Magnification Template Actera hip system CONFORMIS, INC.
21 00810933031350 1080-667 1080-667 Cordera Cup Acetate -120% Magnification Template Cordera Hip System CONFORMIS, INC.
22 00810933031343 1080-665 1080-665 Cordera Cup Acetate - 110% Magnification Template Cordera Hip System CONFORMIS, INC.
23 00810933031336 1080-671 1080-671 Cordera Stem Digital Template Cordera Hip System CONFORMIS, INC.
24 00810933031329 1080-664 1080-664 Cordera Stem Acetate 120% Magnification Template Cordera Hip System CONFORMIS, INC.
25 00810933031312 1080-662 1080-662 Cordera Stem Acetate 110 percent Magnification Template Cordera hip system CONFORMIS, INC.
26 00810933031282 1080-666 1080-666 Cordera Cup Acetate -115% Magnification Template Cordera Hip System CONFORMIS, INC.
27 00810933031275 1080-663 1080-663 Cordera Stem Acetate 115 percent Magnification Template Cordera hip system CONFORMIS, INC.
28 00810482031023 9014-CTL9 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
29 00810482031016 9014-CTL8 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
30 00810482031009 9014-CTL7 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
31 00810482031375 9017-CTP09 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
32 00810482031368 9017-CTP08 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
33 00810482031351 9017-CTP07 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
34 00810482031344 9017-CTP06 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
35 00810482031337 9017-CTP05 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
36 00810482031320 9017-CTP11 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
37 00810482031313 9017-CTP10 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
38 00810482031306 9017-CTL10 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
39 00810482031290 9017-CTL09 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
40 00810482031283 9017-CTL08 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
41 00810482031276 9017-CTL07 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
42 00810482031269 9017-CTL06 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
43 00810482031252 9017-CTL05 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
44 00810482031245 9017-CTL11 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
45 00810482031092 9014-CTP9 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
46 00810482031085 9014-CTP8 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
47 00810482031078 9014-CTP7 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
48 00810482031061 9014-CTP6 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
49 00810482031054 9014-CTP5 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC
50 00810482031047 9014-CTP11 The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. Blustone Synergy Cervical Trial (Slate) BLUSTONE SYNERGY, LLC