No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 07640305160226 | MPF-IN 04 00-N | MPF-IN 04 00-N | TROCAR AWL | KWP,NKB | Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System | 2 | PERLA ® TL MIS |
2 | 07640151087623 | PAD-IM TI 16-S | Posterior Axial Device - Titanium | PEK | Spinous Process Plate | 2 | ROMEO 2 PAD POSTERIOR AXIAL DEVICE | |
3 | 07640151087609 | PAD-IM TI 12-S | Posterior Axial Device - Titanium | PEK | Spinous Process Plate | 2 | ROMEO 2 PAD POSTERIOR AXIAL DEVICE | |
4 | 07640151084073 | ELL-CC MU 43-S | Cross Connector / Multiaxial | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
5 | 07640178975262 | CPF-IN 22 02-N | CPF-IN 22 02-N | Screwdriver Tube | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
6 | 07640151082970 | ELL-DS 07 35-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
7 | 07640151082949 | ELL-DS 06 80-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
8 | 07640151082925 | ELL-DS 06 60-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
9 | 07640450863447 | TRY-IN 51 01-N | TRY-IN 51 01-N | 3D PRINTED HAN | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK ® TI |
10 | 07640151082833 | ELL-DS 55 45-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
11 | 07640450860989 | TLF-SC 00 00-N | TLF-SC 00 00-N | SETSCREW | KWP,NKB | Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System | 2 | PERLA ® TL |
12 | 07640151082819 | ELL-DS 55 35-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
13 | 07640151082772 | ELL-DS 05 40-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
14 | 07640151082703 | ELL-DS 45 25-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
15 | 07640151082680 | ELL-DS 04 40-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
16 | 07640151082659 | ELL-DS 04 25-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
17 | 07640151081928 | ELL-RD 13 50-S | Rod Cobalt Chromium / Straight | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis system | |
18 | 07640305160899 | MPF-PX 65 30-S | MPF-PX 65 30-S | XTAB CANNULATED POLYAXIAL SCREW | KWP,NKB | Appliance, Fixation, Spinal Interlaminal,Thoracolumbosacral Pedicle Screw System | 2 | PERLA ® TL MIS |
19 | 07640178975200 | CPF-IN 17 00-N | CPF-IN 17 00-N | Pusher | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
20 | 07640185341722 | SPE-US 00 40-N | SPE-US 00 40-N | ANGLED TAP | HWX | Tap, Bone | 1 | SCARLET AC-T |
21 | 07640178984981 | MIS-IN 52 10-N | Trocar Handle | HWJ | Awl | 1 | ROMEO 2 MIS | |
22 | 07640178985704 | SPE-US 00 28-N | SPE-US 00 28-N | ROD HOLDER | NKG,KWP | Orthosis, Cervical Pedicle Screw Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
23 | 07640178981584 | JUT-IN 03 12-N | JUT-IN 03 12-N | TRIAL IMPLANT Ti TL | HWT | Template | 1 | JULIET ® INSTRUMENTATION |
24 | 07640178980662 | JUL-LT 6S 8C-S | JUL-LT 6S 8C-S | JUL-LT 6S 8C-S | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | JULIET ® LL |
25 | 07640178975934 | CPF-SS 04 22-S | CPF-SS 04 22-S | NKG,KWP | Orthosis, Cervical Pedicle Screw Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® | |
26 | 07640151081225 | TRY-AC 12 09-S | Cervical Cage / Convex | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
27 | 07640151081010 | TRY-CL 14 12-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
28 | 07640178971301 | ELL-R6 15 50-S | Rod Cobalt Chromium / Prebent | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | ROMEO Posterior Osteosynthesis system | |
29 | 07640151080969 | TRY-CL 14 07-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
30 | 07640151080952 | TRY-CL 14 06-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
31 | 07640151080945 | TRY-CL 14 05-S | Cervical Cage / Lordotic | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK Anterior Intersomatic Cervical cage | |
32 | 07640151112578 | JLL-IN 06 08-N | JLL-IN 06 08-N | PADDLE SHAVER 8 | LWK | Razor, Surgical | 1 | JULIET ® INSTRUMENTATION |
33 | 07640151096304 | CPF-CS 04 52-S | CC PREFERRED ANGLE SCREW | NKG,KWP | Orthosis, Cervical Pedicle Screw Spinal Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® | |
34 | 07640151095239 | CPF-IN 20 00-N | CPF-IN 20 00-N | Rocker | KWP | Appliance, Fixation, Spinal Interlaminal | 2 | PERLA ® |
35 | 07640151092597 | JUL-IN 19 10-N | JUL-IN 19 10-N | Paddle Shaver H10 | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | JULIET INSTRUMENTATION |
36 | 07640139346179 | ELL-RD 10 30-S | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | ||
37 | 07640139345455 | ELL-PS 45 45-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
38 | 07640139345448 | ELL-PS 45 40-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
39 | 07640151089474 | OTO-BC 09 02-N | OTO-BC 09 02-N | RETRACTOR BLADE | GAD | Retractor | 1 | OTELO INSTRUMENTATION |
40 | 07640151087579 | ELL-IN 05 06-N | ELL-IN 05 06-N | K-WIRE BLUNT - NITINOLFINAL TIGHTENER | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO 2 INSTRUMENTATION |
41 | 07640139345424 | ELL-PS 45 30-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
42 | 07640151083021 | ELL-DS 07 55-S | 25D Screw | MNH,MNI,KWP | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Ap Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Appliance, Fixation, Spinal Interlaminal | 2 | ROMEO Posterior Osteosynthesis system | |
43 | 07640151080846 | ELL-IN 01 34-N | ELL-IN 01 34-N | REDUCER T-HANDLE | HWN,MNI,MNH | Instrument, Compression,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolist Instrument, Compression,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 1 | ROMEO 2 INSTRUMENTATION |
44 | 07640139347329 | ELL-RD 30 30-S | Rod Straight | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
45 | 07640139346193 | ELL-RD 10 50-S | Rod Cobalt Chromium / Prebent | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
46 | 07640139347404 | ELL-RD 30 90-S | Rod Straight | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
47 | 07640139347213 | ELL-PS 06 90-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
48 | 07640139345769 | ELL-PS 07 80-S | Polyaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis System | |
49 | 07640139343970 | ELL-MS 45 25-S | Monoaxial Screw | KWP,MNH,MNI | Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixa Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | ROMEO Posterior Osteosynthesis system | |
50 | 07640139340061 | MOS-CA 14 07-S | Cervical Cage | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | TRYPTIK CA ANTERIOR INTERSOMATIC CERVICAL CAGE |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00812388031121 | FA 0208-07 | CTH-617L-07 | Trial Head, 6LL (6mm H x 17mm W x 16mm D), G7 | M6-C | SPINAL KINETICS, INC. |
2 | 00812388031114 | FA 0208-06 | CTH-717-07 | Trial Head, 7L (7mm H x 17mm W x 14mm D), G7 | M6-C | SPINAL KINETICS, INC. |
3 | 00812926027012 | 210-00-007 | Osteotomy Guide | TRILLIANT SURGICAL, LLC | ||
4 | 00812388031107 | FA 0208-05 | CTH-617-07 | Trial Head, 6L (6mm H x 17mm W x 14mm D), G67 | M6-C | SPINAL KINETICS, INC. |
5 | 00812388031091 | FA 0208-04 | CTH-715L-07 | Trial Head, 7ML (7mm H x 15mm W x 15mm D), G7 | M6-C | SPINAL KINETICS, INC. |
6 | 00812388031084 | FA 0208-03 | CTH-615L-07 | Trial Head, 6ML (6mm H x 15mm W x 15mm D), G7 | M6-C | SPINAL KINETICS, INC. |
7 | 00812388031077 | FA 0208-02 | CTH-715-07 | Trial Head, 7M (7mm H x 15mm W x 12.5mm D), G7 | M6-C | SPINAL KINETICS, INC. |
8 | 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. |
9 | 00812388031046 | FA 0190 | CSA-100-07 | Stop Assembly, G7 | M6-C | SPINAL KINETICS, INC. |
10 | 00812388031039 | FA 0189 | CUH-100-07 | Universal Handle Assembly, G7 | M6-C | SPINAL KINETICS, INC. |
11 | 00812388030285 | FA 0191 | CIH-100-06 | Trial Handle, G6 | M6-C | SPINAL KINETICS, INC. |
12 | 00812388030278 | FA 0192-08 | CTH-717L-06 | Trial Head, 7LL (7mm H x 17mm W x 16mm D), G6 | M6-C | SPINAL KINETICS, INC. |
13 | 00812388030261 | FA 0192-06 | CTH-717-06 | Trial Head, 7L (7mm H x 17mm W x 14mm D), G6 | M6-C | SPINAL KINETICS, INC. |
14 | 00812388030254 | FA 0192-04 | CTH-715L-06 | Trial Head, 7ML (7mm H x 15mm W x 15mm D), G6 | M6-C | SPINAL KINETICS, INC. |
15 | 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. |
16 | 00812388030230 | FA 0192-07 | CTH-617L-06 | Trial Head, 6LL (6mm H x 17mm W x 16mm D), G6 | M6-C | SPINAL KINETICS, INC. |
17 | 00812388030216 | FA 0192-03 | CTH-615L-06 | Trial Head, 6ML (6mm H x 15mm W x 15mm D), G6 | M6-C | SPINAL KINETICS, INC. |
18 | 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. |
19 | 00812388030193 | FA 0195-02 | CFT-200L-06 | Footprint Template, L/LL, G6 | M6-C | SPINAL KINETICS, INC. |
20 | 00812388030186 | FA 0195-01 | CFT-200M-06 | Footprint Template, M/ML, G6 | M6-C | SPINAL KINETICS, INC. |
21 | 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. |
22 | 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. |
23 | 00810933031367 | 1080-672 | 1080-672 | Cordera Cup Digital Template | Cordera Hip System | CONFORMIS, INC. |
24 | 00810933031404 | 1080-673 | 1080-673 | Actera Stem Digital Template | Actera hip system | CONFORMIS, INC. |
25 | 00810933031398 | 1080-670 | 1080-670 | Actera Stem Acetate -120% Magnification Template | Actera hip system | CONFORMIS, INC. |
26 | 00810933031381 | 1080-669 | 1080-669 | Actera Stem Acetate -115% Magnification Template | Actera hip system | CONFORMIS, INC. |
27 | 00810933031374 | 1080-668 | 1080-668 | Actera Stem Acetate -110% Magnification Template | Actera hip system | CONFORMIS, INC. |
28 | 00810933031350 | 1080-667 | 1080-667 | Cordera Cup Acetate -120% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
29 | 00810933031343 | 1080-665 | 1080-665 | Cordera Cup Acetate - 110% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
30 | 00810933031336 | 1080-671 | 1080-671 | Cordera Stem Digital Template | Cordera Hip System | CONFORMIS, INC. |
31 | 00810933031329 | 1080-664 | 1080-664 | Cordera Stem Acetate 120% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
32 | 00810933031312 | 1080-662 | 1080-662 | Cordera Stem Acetate 110 percent Magnification Template | Cordera hip system | CONFORMIS, INC. |
33 | 00810933031282 | 1080-666 | 1080-666 | Cordera Cup Acetate -115% Magnification Template | Cordera Hip System | CONFORMIS, INC. |
34 | 00810933031275 | 1080-663 | 1080-663 | Cordera Stem Acetate 115 percent Magnification Template | Cordera hip system | CONFORMIS, INC. |
35 | 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 | |
36 | 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 | |
37 | 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 | |
38 | 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 | |
39 | 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 | |
40 | 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 | |
41 | 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 | |
42 | 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 | |
43 | 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 | |
44 | 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 | |
45 | 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 | |
46 | 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 | |
47 | 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 | |
48 | 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 | |
49 | 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 | |
50 | 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 |