Other products from "PAJUNK GMBH MEDIZINTECHNOLOGIE"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 04048223117422 561185-31A 561185-31A 561185-31A CAZ Anesthesia conduction kit 2 SONOLONG ECHO
2 14048223041380 201285-42E 201285-42E E-Cath Stimulong acc. Tsui BSO CATHETER, CONDUCTION, ANESTHETIC 2 E-Cath Stimulong acc. Tsui
3 14048223041366 241285-42E 241285-42E E-Cath Stimulong acc. Tsui BSO CATHETER, CONDUCTION, ANESTHETIC 2 E-Cath Stimulong acc. Tsui
4 14048223037093 001280-95 001280-95 SonoBlock II Facet 20G (0,90) x 100mm SonoBlock II Facet 20G (0,90) x 100mm with injection tube BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoBlock II Facet
5 14048223036539 001285-75 001285-75 SonoPlex II Facet 24G (0,55) x 30mm SonoPlex II Facet 24G (0,55) x 30mm with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
6 14048223036522 001285-76 001285-76 SonoPlex II Facet 20G (0,90) x 150mm SonoPlex II Facet 20G (0,90) x 150mm with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
7 14048223036515 001285-78 001285-78 SonoPlex II Facet 24G (0,55) x 40mm, SonoPlex II Facet 24G (0,55) x 40mm, with injection tube and connecting cabe BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
8 14048223034269 241185-42E 241185-42E E-Cath Stimulong acc. Tsui BSO CATHETER, CONDUCTION, ANESTHETIC 2 E-Cath Stimulong acc. Tsui
9 14048223034245 201185-42E 201185-42E E-Cath Stimulong acc. Tsui BSO CATHETER, CONDUCTION, ANESTHETIC 2 E-Cath Stimulong acc. Tsui
10 14048223033538 001280-72 001280-72 SonoBlock II Facet 20G (0,90) x 120mm SonoBlock II Facet 20G (0,90) x 120mm with injection tube BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoBlock II Facet
11 14048223033286 1285-3F150 1285-3F150 SonoTAP II 21G x 150mm wit bevel tip and SonoTAP II 21G x 150mm wit bevel tip and Cornerstone Reflectors BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoTAP II
12 14048223033224 1285-3F110 1285-3F110 SonoTAP II 21G x 110mm with bevel tip and SonoTAP II 21G x 110mm with bevel tip and Cornerstone Reflectors BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoTAP II
13 14048223033217 1285-3E080 1285-3E080 SonoTAP II 22G x 80mm with bevel tip and SonoTAP II 22G x 80mm with bevel tip and Cornerstone Reflectors BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoTAP II
14 14048223033200 1285-3E050 1285-3E050 SonoTAP II 22G x 50mm with bevel tip and SonoTAP II 22G x 50mm with bevel tip and Cornerstone Reflectors BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoTAP II
15 14048223033194 001280-71 001280-71 SonoBlock II Facet 22G (0,70) x 80mm SonoBlock II Facet 22G (0,70) x 80mm with injection tube BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoBlock II Facet
16 14048223033187 001280-77 001280-77 SonoBlock II Facet 21G (0,80) x 100mm SonoBlock II Facet 21G (0,80) x 100mm with injection tube BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoBlock II Facet
17 14048223033170 001280-74 001280-74 SonoBlock II Facet 22G (0,70) x 50mm SonoBlock II Facet 22G (0,70) x 50mm with injection tube BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoBlock II Facet
18 14048223033132 001285-77 001285-77 SonoPlex II Facet 21G (0,80) x 100mm, SonoPlex II Facet 21G (0,80) x 100mm, with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
19 14048223033125 001285-74 001285-74 SonoPlex II Facet 22G (0,70) x 50mm, SonoPlex II Facet 22G (0,70) x 50mm, with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
20 14048223033118 001285-71 001285-71 SonoPlex II Facet 22G (0,70) x 80mm, SonoPlex II Facet 22G (0,70) x 80mm, with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
21 14048223032258 001267-76 001267-76 SonoPlex II Facet S NRFit 20G (0,90) x 150mm, Facet tip S SonoPlex II Facet S NRFit 20G (0,90) x 150mm, Facet tip S with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet S NRFit
22 14048223032241 001267-72 001267-72 SonoPlex II Facet S NRFit 20G (0,90) x 120mm, Facet tip S SonoPlex II Facet S NRFit 20G (0,90) x 120mm, Facet tip S with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet S NRFit
23 14048223032234 001267-77 001267-77 SonoPlex II Facet S NRFit 21G (0,80) x 100mm, Facet tip S SonoPlex II Facet S NRFit 21G (0,80) x 100mm, Facet tip S with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet S NRFit
24 14048223032227 001267-71 001267-71 SonoPlex II Facet S NRFit 22G (0,70) x 80mm, Facet tip S SonoPlex II Facet S NRFit 22G (0,70) x 80mm, Facet tip S with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet S NRFit
25 14048223032210 001267-74 001267-74 SonoPlex II Facet S NRFit 22G (0,70) x 50mm, Facet tip S SonoPlex II Facet S NRFit 22G (0,70) x 50mm, Facet tip S with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet S NRFit
26 14048223032203 001267-70 001267-70 SonoPlex II Facet S NRFit 22G (0,70) x 40mm, Facet tip S SonoPlex II Facet S NRFit 22G (0,70) x 40mm, Facet tip S with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet S NRFit
27 14048223031800 001285-70 001285-70 SonoPlex II Facet 22G (0,70) x 40mm SonoPlex II Facet 22G (0,70) x 40mm with injection tube and connecting cable BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SonoPlex II Facet
28 14048223031657 001163-30E 001163-30E SPROTTE® NRFit 24G x 1 3/8" (35mm) sterile BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
29 14048223030353 031163-27A 031163-27A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
30 14048223030346 211163-27A 211163-27A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
31 14048223030339 261163-29A 261163-29A SPROTTE® NRFit 25G x 6" (150mm) BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
32 14048223030315 211163-29A 211163-29A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
33 14048223030308 0051163-30 0051163-30 SPROTTE® NRFit 24G x 8" (200mm) SPROTTE® NRFit 24G x 8" (200mm) with IntroDucer NRFit 40mm BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
34 14048223030292 001163-30D 001163-30D SPROTTE® NRFit 24G x 1" (25mm) BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
35 14048223030261 221163-30C 221163-30C SPROTTE® NRFit 22G x 4" (103mm) SPROTTE® NRFit 22G x 4" (103mm) with IntroDucer NRFit 40mm BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
36 14048223030254 001163-30C 001163-30C SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
37 14048223029913 021163-27A 021163-27A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
38 14048223029821 001163-30A 001163-30A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
39 14048223029777 001163-38F 001163-38F Spinal Manometer NRFit FMJ MANOMETER, SPINAL-FLUID 2 Spinal Manometer NRFit
40 14048223027025 231163-27A 231163-27A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
41 14048223027018 041163-27A 041163-27A SPROTTE® NRFit 27G x 4" (103mm) SPROTTE® NRFit 27G x 4" (103mm) with IntroDucer NRFit 40mm BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
42 14048223027001 061163-29A 061163-29A SPROTTE® NRFit 25G x 6" (150mm) SPROTTE® NRFit 25G x 6" (150mm) with IntroDucer NRFit 40mm BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
43 14048223026998 031163-29A 031163-29A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
44 14048223026981 051163-29A 051163-29A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
45 14048223026974 041163-29A 041163-29A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
46 14048223026967 501163-29A 501163-29A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
47 14048223026950 021163-29A 021163-29A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
48 14048223026943 001163-29E 001163-29E SPROTTE® NRFit 25G x 1 3/8" (35mm) BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
49 14048223026936 131163-30A 131163-30A SPROTTE® NRFit 24G x 6" (150mm) SPROTTE® NRFit 24G x 6" (150mm) with IntroDucer NRFit 40mm BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
50 14048223026929 041163-30A 041163-30A SPROTTE® NRFit BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) SPROTTE® NRFit
Other products with the same Product Code "MDM"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 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.
2 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.
3 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.
4 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.
5 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.
6 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.
7 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.
8 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.
9 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.
10 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.
11 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.
12 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.
13 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.
14 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.
15 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.
16 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.
17 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.
18 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.
19 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.
20 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.
21 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.
22 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.
23 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.
24 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.
25 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.
26 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.
27 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.
28 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.
29 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.
30 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.
31 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.
32 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.
33 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.
34 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.
35 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.
36 00814008025916 PD-1000T-098 Open 7.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 7.5MM 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.
37 00814008025909 PD-1000T-097 Open 6.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 6.5MM 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.
38 00814008025893 PD-1000T-096 Open 5.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 5.5MM 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.
39 00814008025886 PD-1000T-095 Open 4.75MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in t Open 4.75MM 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.
40 00814008025879 PD-1000T-003 MIS Third Dilator. The FOCUS Pedicle Screw System is intended for use in the no MIS Third Dilator. 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 00814008025862 PD-1000T-002 MIS Second Dilator. The FOCUS Pedicle Screw System is intended for use in the n MIS Second Dilator. 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 00814008025855 PD-1000T-001 MIS Initial Dilator. The FOCUS Pedicle Screw System is intended for use in the MIS Initial Dilator. 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 00814008025848 PD-1000T-004 MIS Final Dilator, Smooth. The FOCUS Pedicle Screw System is intended for use i MIS Final Dilator, Smooth. 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 00814008025824 PD-1000T-018 MIS 8.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 8.5MM Tap, Cannulated. 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 00814008025817 PD-1000T-017 MIS 7.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 7.5MM Tap, Cannulated. 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 00814008025800 PD-1000T-016 MIS 6.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 6.5MM Tap, Cannulated. 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 00814008025794 PD-1000T-015 MIS 5.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 5.5MM Tap, Cannulated. 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 00814008025787 PD-1000T-014 MIS 4.75MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use MIS 4.75MM Tap, Cannulated. 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 00814008025770 PD-1000T-051 MIS Rod Length Calipers. The FOCUS Pedicle Screw System is intended for use in MIS Rod Length Calipers. 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 00814008025763 PD-1000T-050 MIS Pedicle Screw Driver. The FOCUS Pedicle Screw System is intended for use in MIS Pedicle 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.