| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | M684EPT6514LWD1 | EPT6514LWD | EPT6514LWD | HWT | TEMPLATE | 1 | PS | |
| 2 | M684PNV036111 | PNV03611 | PNV03611 | JWH,MBH,OOG | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 3 | M684PHA062121 | PHA06212 | PHA06212 | LPH,LZO | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented | 2 | PROCOTYL | |
| 4 | M684KTIBTL2U1 | KTIBTL2U | KTIBTL2U | HWT | TEMPLATE | 1 | ADVANCE® | |
| 5 | M684KTTINP251 | KTTINP25 | KTTINP25 | HRY,JWH | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER,PROSTH PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | ADVANCE | |
| 6 | M684KTRLBF601 | KTRLBF60 | KTRLBF60 | HWT | TEMPLATE | 1 | ODYSSEY® | |
| 7 | M684KITLL1071 | KITLL107 | KITLL107 | HWT | TEMPLATE | 1 | ADVANCE® | |
| 8 | M684KIDT414L1 | KIDT414L | KIDT414L | HWT | TEMPLATE | 1 | ADVANCE® | |
| 9 | M684KIDT412R1 | KIDT412R | KIDT412R | HWT | TEMPLATE | 1 | ADVANCE® | |
| 10 | M684KFPCMR101 | KFPCMR10 | KFPCMR10 | HWT | TEMPLATE | 1 | ODYSSEY® | |
| 11 | M684ETRKN4SL1 | ETRKN4SL | ETRKN4SL | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | EVOLUTION® | |
| 12 | M684EAT4212L1 | EAT4212L | EAT4212L | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 13 | M684EFSAN1PR1 | EFSAN1PR | EFSAN1PR | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | EVOLUTION | |
| 14 | M684EAT7517R1 | EAT7517R | EAT7517R | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 15 | M684EAT6310R1 | EAT6310R | EAT6310R | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 16 | M684EAT5217R1 | EAT5217R | EAT5217R | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 17 | M684EFXPNP4L1 | EFXPNP4L | EFXPNP4L | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | EVOLUTION | |
| 18 | M684E63043RL1 | E63043RL | E63043RL | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 19 | M684E63048RL1 | E63048RL | E63048RL | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 20 | M684E63042RL1 | E63042RL | E63042RL | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 21 | M684E17046821 | E1704682 | E1704682 | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 22 | M684DNFLTRA11 | DNFLTRA1 | DNFLTRA1 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DYNASTY® | |
| 23 | M684515618141 | 51561814 | 51561814 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | MicroPort | |
| 24 | M684400010581 | 40001058 | 40001058 | HWT | TEMPLATE | 1 | INTERSEAL® | |
| 25 | M6843304LJ501 | 3304LJ50 | 3304LJ50 | HWT | TEMPLATE | 1 | DYNASTY® | |
| 26 | M6843658XR151 | 3658XR15 | 3658XR15 | HWT | TEMPLATE | 1 | LINEAGE® | |
| 27 | M684333300201 | 33330020 | 33330020 | HWA | IMPACTOR | 1 | DYNASTY® | |
| 28 | M6843000AG011 | 3000AG01 | 3000AG01 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | INTERSEAL® | |
| 29 | M684188160521 | 18816052 | 18816052 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | Advantim | |
| 30 | M684184191141 | 18419114 | 18419114 | HWT | TEMPLATE | 1 | ORTHOLOC® | |
| 31 | M684180700421 | 18070042 | 18070042 | HWT | TEMPLATE | 1 | SLR | |
| 32 | M684184101331 | 18410133 | 18410133 | FZX | Guide, surgical, instrument | 1 | Advantium | |
| 33 | M684PNV040491 | PNV04049 | PNV04049 | OOG,MBH,JWH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SE Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 34 | M684PNV040481 | PNV04048 | PNV04048 | JWH,MBH,OOG | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 35 | M684PNV040471 | PNV04047 | PNV04047 | MBH,JWH,OOG | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 36 | M684PNV040461 | PNV04046 | PNV04046 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 37 | M684PNV040451 | PNV04045 | PNV04045 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 38 | M684PNV040441 | PNV04044 | PNV04044 | MBH,JWH,OOG | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 39 | M684PNV040431 | PNV04043 | PNV04043 | JWH,MBH,OOG | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 40 | M684PNV040421 | PNV04042 | PNV04042 | OOG,MBH,JWH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SE Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 41 | M684PNV040411 | PNV04041 | PNV04041 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 42 | M684PNV040401 | PNV04040 | PNV04040 | MBH,JWH,OOG | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 43 | M684PNV040391 | PNV04039 | PNV04039 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 44 | M684PNV040381 | PNV04038 | PNV04038 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 45 | M684PNV040371 | PNV04037 | PNV04037 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 46 | M684PNV040361 | PNV04036 | PNV04036 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 47 | M684PNV040351 | PNV04035 | PNV04035 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 48 | M684PNV040341 | PNV04034 | PNV04034 | OOG,JWH,MBH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEM Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 49 | M684PNV040331 | PNV04033 | PNV04033 | OOG,MBH,JWH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SE Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 50 | M684PNV040321 | PNV04032 | PNV04032 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00812388030285 | FA 0191 | CIH-100-06 | Trial Handle, G6 | M6-C | SPINAL KINETICS, INC. |
| 2 | 00812388030278 | FA 0192-08 | CTH-717L-06 | Trial Head, 7LL (7mm H x 17mm W x 16mm D), G6 | M6-C | SPINAL KINETICS, INC. |
| 3 | 00812388030261 | FA 0192-06 | CTH-717-06 | Trial Head, 7L (7mm H x 17mm W x 14mm D), G6 | M6-C | SPINAL KINETICS, INC. |
| 4 | 00812388030254 | FA 0192-04 | CTH-715L-06 | Trial Head, 7ML (7mm H x 15mm W x 15mm D), G6 | M6-C | SPINAL KINETICS, INC. |
| 5 | 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. |
| 6 | 00812388030230 | FA 0192-07 | CTH-617L-06 | Trial Head, 6LL (6mm H x 17mm W x 16mm D), G6 | M6-C | SPINAL KINETICS, INC. |
| 7 | 00812388030216 | FA 0192-03 | CTH-615L-06 | Trial Head, 6ML (6mm H x 15mm W x 15mm D), G6 | M6-C | SPINAL KINETICS, INC. |
| 8 | 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. |
| 9 | 00812388030193 | FA 0195-02 | CFT-200L-06 | Footprint Template, L/LL, G6 | M6-C | SPINAL KINETICS, INC. |
| 10 | 00812388030186 | FA 0195-01 | CFT-200M-06 | Footprint Template, M/ML, G6 | M6-C | SPINAL KINETICS, INC. |
| 11 | 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. |
| 12 | 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. |
| 13 | 00810933031367 | 1080-672 | 1080-672 | Cordera Cup Digital Template | Cordera Hip System | CONFORMIS, INC. |
| 14 | 00810933031404 | 1080-673 | 1080-673 | Actera Stem Digital Template | Actera hip system | CONFORMIS, INC. |
| 15 | 00810933031398 | 1080-670 | 1080-670 | Actera Stem Acetate -120% Magnification Template | Actera hip system | CONFORMIS, INC. |
| 16 | 00810933031381 | 1080-669 | 1080-669 | Actera Stem Acetate -115% Magnification Template | Actera hip system | CONFORMIS, INC. |
| 17 | 00810933031374 | 1080-668 | 1080-668 | Actera Stem Acetate -110% Magnification Template | Actera hip system | CONFORMIS, INC. |
| 18 | 00810933031350 | 1080-667 | 1080-667 | Cordera Cup Acetate -120% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
| 19 | 00810933031343 | 1080-665 | 1080-665 | Cordera Cup Acetate - 110% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
| 20 | 00810933031336 | 1080-671 | 1080-671 | Cordera Stem Digital Template | Cordera Hip System | CONFORMIS, INC. |
| 21 | 00810933031329 | 1080-664 | 1080-664 | Cordera Stem Acetate 120% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
| 22 | 00810933031312 | 1080-662 | 1080-662 | Cordera Stem Acetate 110 percent Magnification Template | Cordera hip system | CONFORMIS, INC. |
| 23 | 00810933031282 | 1080-666 | 1080-666 | Cordera Cup Acetate -115% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
| 24 | 00810933031275 | 1080-663 | 1080-663 | Cordera Stem Acetate 115 percent Magnification Template | Cordera hip system | CONFORMIS, INC. |
| 25 | 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 | |
| 26 | 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 | |
| 27 | 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 | |
| 28 | 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 | |
| 29 | 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 | |
| 30 | 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 | |
| 31 | 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 | |
| 32 | 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 | |
| 33 | 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 | |
| 34 | 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 | |
| 35 | 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 | |
| 36 | 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 | |
| 37 | 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 | |
| 38 | 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 | |
| 39 | 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 | |
| 40 | 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 | |
| 41 | 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 | |
| 42 | 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 | |
| 43 | 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 | |
| 44 | 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 | |
| 45 | 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 | |
| 46 | 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 | |
| 47 | 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 | |
| 48 | 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 | |
| 49 | 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 | |
| 50 | 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 |