No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00190446735922 | 342-13-705 | EMPOWR 3D KNEETM INS, 5R 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
2 | 00190446735915 | 341-13-705 | EMPOWR 3D KNEETM INS, 5L 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
3 | 00190446735762 | 341-11-702 | EMPOWR 3D KNEETM INS, 2L 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
4 | 00190446302636 | 414922 | 2.0 AND 2.7MM SCREW DRIVER HANDLE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | DJO SURGICAL | |
5 | 00190446747482 | 800-05-096 | DJO EMPOWR REVISION KNEE, FEMORAL TRIAL LOCATOR, SZ 6-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
6 | 00190446747468 | 800-05-095 | DJO EMPOWR REVISION KNEE, FEMORAL TRIAL LOCATOR, SZ 2-5 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
7 | 00190446745266 | 800-05-094 | DJO EMPOWR REVISION KNEE, FEMORAL FLEXION TOWER 0/3 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
8 | 00190446302605 | 414916 | DISCOVERY XS HUM RES TEMPLATE | HWT | TEMPLATE | 1 | DJO SURGICAL | |
9 | 00190446736165 | 342-13-711 | EMPOWR 3D KNEETM INS, 11R 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
10 | 00190446302582 | 414913 | DISCOVERY XS FOSSA REAMER | HTO | REAMER | 1 | DJO SURGICAL | |
11 | 00190446736158 | 341-13-711 | EMPOWR 3D KNEETM INS, 11L 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
12 | 00190446302575 | 414912 | DISCOVERY 5 STEP FOSSA REAMER | HTO | REAMER | 1 | DJO SURGICAL | |
13 | 00190446736141 | 342-11-711 | EMPOWR 3D KNEETM INS, 11R 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
14 | 00190446736134 | 341-11-711 | EMPOWR 3D KNEETM INS, 11L 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
15 | 00190446736127 | 342-13-710 | EMPOWR 3D KNEETM INS, 10R 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
16 | 00190446736110 | 341-13-710 | EMPOWR 3D KNEETM INS, 10L 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
17 | 00190446302292 | 414868 | DISC 2.5MM RIGHT ULNA RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
18 | 00190446736103 | 342-11-710 | EMPOWR 3D KNEETM INS, 10R 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
19 | 00190446302285 | 414867 | DISC 2.5MM LEFT ULNA RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
20 | 00190446736097 | 341-11-710 | EMPOWR 3D KNEETM INS, 10L 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
21 | 00190446736080 | 342-13-709 | EMPOWR 3D KNEETM INS, 9R 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
22 | 00190446736073 | 341-13-709 | EMPOWR 3D KNEETM INS, 9L 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
23 | 00190446736066 | 342-11-709 | EMPOWR 3D KNEETM INS, 9R 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
24 | 00190446736059 | 341-11-709 | EMPOWR 3D KNEETM INS, 9L 11MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
25 | 00190446736042 | 342-13-708 | EMPOWR 3D KNEETM INS, 8R 13MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
26 | 00190446736035 | 341-13-708 | EMPOWR 3D KNEETM INS, 8L 13MM, VE | JWH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | DJO SURGICAL | |
27 | 00190446736028 | 342-11-708 | EMPOWR 3D KNEETM INS, 8R 11MM, VE | OIY,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
28 | 00190446764335 | 803-03-241 | MODULAR T-HANDLE, LINEAR PLUS | LXH | Orthopedic manual surgical instrument | 1 | DJO SURGICAL | |
29 | 00190446764274 | 800-99-161 | EMPOWR REVISION KNEE, HALF-TRAY LID | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DJO SURGICAL | |
30 | 00190446757672 | 800-99-160 | EMPOWR REVISION KNEE, OUTLIER TRAY, SZ: 2-3, 10-11 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DJO SURGICAL | |
31 | 00190446301950 | 414820 | DISC 3.5MM DIST HUMERAL RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
32 | 00190446757665 | 800-99-159 | EMPOWR REVISION KNEE, CORE TRAY, SZ: 4-9 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DJO SURGICAL | |
33 | 00190446301912 | 414815 | DISC 3.5X124MM PROX HUM RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
34 | 00190446754282 | 800-05-098 | DJO EMPOWR REVISION KNEE, STEM EXTENDER TRIAL, 15MM X 25MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
35 | 00190446753957 | 800-05-097 | DJO EMPOWR REVISION KNEE, ANTERIOR CUT GUIDE, SIZE 6-11 | FZX | Guide, surgical, instrument | 1 | DJO SURGICAL | |
36 | 00190446750734 | 800-05-093 | DJO EMPOWR REVISION KNEE, 3.5MM BALL END HEX DRIVER | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
37 | 00190446735663 | 800-05-122 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 10/11, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
38 | 00190446735656 | 800-05-121 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 8/9, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
39 | 00190446735649 | 800-05-120 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 6/7, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
40 | 00190446301905 | 414814 | DISC 3.5X84MM PROX HUM RASP | HTQ | BROACH | 1 | DJO SURGICAL | |
41 | 00190446735632 | 800-05-119 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 4/5, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
42 | 00190446735625 | 800-05-118 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 2/3, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
43 | 00190446735618 | 800-05-117 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 10/11, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
44 | 00190446735601 | 800-05-116 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 8/9, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
45 | 00190446296652 | 803-42-44K | Trial Liner, EMPOWR Acetabular, 10°, 44K | FZX | Guide, surgical, instrument | 1 | DJO SURGICAL | |
46 | 00190446735595 | 800-05-115 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 6/7, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
47 | 00190446735588 | 800-05-114 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 4/5, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
48 | 00190446735571 | 800-05-113 | DJO EMPOWR REVISION KNEE, DISTAL AUG TRIALS, SZ 2/3, 5MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
49 | 00190446735564 | 800-05-112 | DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 10/11, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL | |
50 | 00190446735557 | 800-05-111 | DJO EMPOWR REVISION KNEE, POST AUG TRIALS, SZ 8/9, 10MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | DJO SURGICAL |
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 |