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™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00810933031367 | 1080-672 | 1080-672 | Cordera Cup Digital Template | Cordera Hip System | CONFORMIS, INC. |
2 | 00810933031404 | 1080-673 | 1080-673 | Actera Stem Digital Template | Actera hip system | CONFORMIS, INC. |
3 | 00810933031398 | 1080-670 | 1080-670 | Actera Stem Acetate -120% Magnification Template | Actera hip system | CONFORMIS, INC. |
4 | 00810933031381 | 1080-669 | 1080-669 | Actera Stem Acetate -115% Magnification Template | Actera hip system | CONFORMIS, INC. |
5 | 00810933031374 | 1080-668 | 1080-668 | Actera Stem Acetate -110% Magnification Template | Actera hip system | CONFORMIS, INC. |
6 | 00810933031350 | 1080-667 | 1080-667 | Cordera Cup Acetate -120% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
7 | 00810933031343 | 1080-665 | 1080-665 | Cordera Cup Acetate - 110% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
8 | 00810933031336 | 1080-671 | 1080-671 | Cordera Stem Digital Template | Cordera Hip System | CONFORMIS, INC. |
9 | 00810933031329 | 1080-664 | 1080-664 | Cordera Stem Acetate 120% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
10 | 00810933031312 | 1080-662 | 1080-662 | Cordera Stem Acetate 110 percent Magnification Template | Cordera hip system | CONFORMIS, INC. |
11 | 00810933031282 | 1080-666 | 1080-666 | Cordera Cup Acetate -115% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
12 | 00810933031275 | 1080-663 | 1080-663 | Cordera Stem Acetate 115 percent Magnification Template | Cordera hip system | CONFORMIS, INC. |
13 | 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 | |
14 | 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 | |
15 | 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 | |
16 | 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 | |
17 | 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 | |
18 | 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 | |
19 | 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 | |
20 | 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 | |
21 | 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 | |
22 | 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 | |
23 | 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 | |
24 | 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 | |
25 | 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 | |
26 | 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 | |
27 | 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 | |
28 | 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 | |
29 | 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 | |
30 | 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 | |
31 | 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 | |
32 | 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 | |
33 | 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 | |
34 | 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 | |
35 | 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 | |
36 | 00810482031030 | 9014-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 parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
37 | 00810482030996 | 9014-CTL6 | 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 | |
38 | 00810482030989 | 9014-CTL5 | 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 | |
39 | 00810482030972 | 9014-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 parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
40 | 00810482030965 | 9014-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 parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
41 | 00810482030767 | 9000-SP15 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
42 | 00810482030750 | 9000-SP14 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
43 | 00810482030743 | 9000-SP13 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
44 | 00810482030736 | 9000-SP12 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
45 | 00810482030729 | 9000-SP11 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
46 | 00810482030712 | 9000-SP10 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
47 | 00810482030705 | 9000-SP09 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
48 | 00810482030699 | 9000-SP08 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
49 | 00810482030675 | 9000-SP07 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
50 | 00810074751131 | LSTS-SM0614-SH | LSTS-SM0614-SH | 4WEB Medical | 4WEB MEDICAL |