Other products from "MICROPORT ORTHOPEDICS INC."
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
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16 00814008029822 PD-1000T-110 Tower Dis-Engage Instrument. The FOCUS Pedicle Screw System is intended for use Tower Dis-Engage Instrument. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00814008029815 PD-1000T-109 Small Ratcheting T-Handle. The FOCUS Pedicle Screw System is intended for use i Small Ratcheting T-Handle. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00814008029778 PD-1000T-112 Awl Small. The FOCUS Pedicle Screw System is intended for use in the non-cervic Awl Small. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00814008029754 PD-1000T-108 Cross Connector Screw Driver. The FOCUS Pedicle Screw System is intended for us Cross Connector Screw Driver. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00814008029747 PD-1000T-107 Rod Template. The FOCUS Pedicle Screw System is intended for use in the non-cer Rod Template. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00814008026289 PD-1000T-105 Linear Persuader Counter Torque. The FOCUS Pedicle Screw System is intended for Linear Persuader Counter Torque. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
22 00814008026265 PD-1000T-043 Drill, for 7.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 7.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
23 00814008026258 PD-1000T-042 Drill, for 6.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 6.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
24 00814008026227 PD-1000T-074 Open Head Turner. The FOCUS Pedicle Screw System is intended for use in the non Open Head Turner. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
25 00814008026210 PD-1000T-073 Open Rod De-Rotator. The FOCUS Pedicle Screw System is intended for use in the Open Rod De-Rotator. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
26 00814008026166 PD-1000T-068 Open Rod Holder. The FOCUS Pedicle Screw System is intended for use in the non- Open Rod Holder. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
27 00814008026159 PD-1000T-067 Open (Counter) Anti-Torque. The FOCUS Pedicle Screw System is intended for use Open (Counter) Anti-Torque. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
28 00814008026142 PD-1000T-066 Open Rod Rocker. The FOCUS Pedicle Screw System is intended for use in the non- Open Rod Rocker. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
29 00814008026135 PD-1000T-065 Open Rod Pusher. The FOCUS Pedicle Screw System is intended for use in the non- Open Rod Pusher. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
30 00814008026128 PD-1000T-064 Rod Cutter. The FOCUS Pedicle Screw System is intended for use in the non-cervi Rod Cutter. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
31 00814008026111 PD-1000T-063 Open French Rod Bender. The FOCUS Pedicle Screw System is intended for use in t Open French Rod Bender. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
32 00814008026104 PD-1000T-103 Open Persuader, Linear. The FOCUS Pedicle Screw System is intended for use in t Open Persuader, Linear. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
33 00814008026098 PD-1000T-062 Open Persuader, Offset. The FOCUS Pedicle Screw System is intended for use in t Open Persuader, Offset. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
34 00814008026081 PD-1000T-061 Set Screw Driver (Double End). The FOCUS Pedicle Screw System is intended for u Set Screw Driver (Double End). The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
35 00814008026074 PD-1000T-060 Open Pedical Screw Driver. The FOCUS Pedicle Screw System is intended for use i Open Pedical Screw Driver. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
36 00814008026067 PD-1000T-059 Distractor, Titanium. The FOCUS Pedicle Screw System is intended for use in the Distractor, Titanium. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
37 00814008026050 PD-1000T-055 Compressor, Titanium. The FOCUS Pedicle Screw System is intended for use in the Compressor, Titanium. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
38 00814008026043 PD-1000T-102 Open Probe, Lenke, Small. The FOCUS Pedicle Screw System is intended for use in Open Probe, Lenke, Small. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
39 00814008026036 PD-1000T-101 Open Probe, Duckbill, Small. The FOCUS Pedicle Screw System is intended for use Open Probe, Duckbill, Small. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
40 00814008026029 PD-1000T-054 Open Probe, Lenke, Large. The FOCUS Pedicle Screw System is intended for use in Open Probe, Lenke, Large. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
41 00814008026012 PD-1000T-053 Open Probe, Duckbill, Large. The FOCUS Pedicle Screw System is intended for use Open Probe, Duckbill, Large. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
42 00814008026005 PD-1000T-100 Open Sounder, Straight Thick. The FOCUS Pedicle Screw System is intended for us Open Sounder, Straight Thick. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
43 00814008025992 PD-1000T-052 Open Sounder, Straight Slim. The FOCUS Pedicle Screw System is intended for use Open Sounder, Straight Slim. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
44 00814008025985 PD-1000T-044 Drill, for 8.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 8.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
45 00814008025978 PD-1000T-041 Drill, for 5.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 5.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
46 00814008025961 PD-1000T-040 Drill, for 4.75MM. The FOCUS Pedicle Screw System is intended for use in the no Drill, for 4.75MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
47 00814008025954 PD-1000T-027 Open Awl. The FOCUS Pedicle Screw System is intended for use in the non-cervica Open Awl. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
48 00814008025947 PD-1000T-024 Open Reduction Tab Breaker. The FOCUS Pedicle Screw System is intended for use Open Reduction Tab Breaker. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
49 00814008025930 PD-1000T-022 Final Tightener, Set Screw. The FOCUS Pedicle Screw System is intended for use Final Tightener, Set Screw. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
50 00814008025923 PD-1000T-099 Open 8.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 8.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.