No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00889024233638 | 42-5112-004-10 | 42-5112-004-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
2 | 00889024233621 | 42-5112-003-20 | 42-5112-003-20 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
3 | 00889024233614 | 42-5112-003-18 | 42-5112-003-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
4 | 00889024233607 | 42-5112-003-16 | 42-5112-003-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
5 | 00889024233591 | 42-5112-003-14 | 42-5112-003-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
6 | 00889024233584 | 42-5112-003-13 | 42-5112-003-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
7 | 00889024233577 | 42-5112-003-12 | 42-5112-003-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
8 | 00889024233560 | 42-5112-003-11 | 42-5112-003-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
9 | 00889024233553 | 42-5112-003-10 | 42-5112-003-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
10 | 00889024233546 | 42-5112-002-20 | 42-5112-002-20 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
11 | 00889024233539 | 42-5112-002-18 | 42-5112-002-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
12 | 00889024233522 | 42-5112-002-16 | 42-5112-002-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
13 | 00889024233515 | 42-5112-002-14 | 42-5112-002-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
14 | 00889024233508 | 42-5112-002-13 | 42-5112-002-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
15 | 00889024233492 | 42-5112-002-12 | 42-5112-002-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
16 | 00889024233485 | 42-5112-002-11 | 42-5112-002-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
17 | 00889024233478 | 42-5112-002-10 | 42-5112-002-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
18 | 00889024233461 | 42-5112-001-20 | 42-5112-001-20 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
19 | 00889024233454 | 42-5112-001-18 | 42-5112-001-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
20 | 00889024233447 | 42-5112-001-16 | 42-5112-001-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
21 | 00889024233430 | 42-5112-001-14 | 42-5112-001-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
22 | 00889024233423 | 42-5112-001-13 | 42-5112-001-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
23 | 00889024233416 | 42-5112-001-12 | 42-5112-001-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
24 | 00889024233409 | 42-5112-001-11 | 42-5112-001-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
25 | 00889024233393 | 42-5112-001-10 | 42-5112-001-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
26 | 00889024233386 | 42-5110-007-18 | 42-5110-007-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
27 | 00889024233379 | 42-5110-007-16 | 42-5110-007-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
28 | 00889024233362 | 42-5110-007-14 | 42-5110-007-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
29 | 00889024233355 | 42-5110-007-13 | 42-5110-007-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
30 | 00889024233348 | 42-5110-007-12 | 42-5110-007-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
31 | 00889024233331 | 42-5110-007-11 | 42-5110-007-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
32 | 00889024233324 | 42-5110-007-10 | 42-5110-007-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
33 | 00889024233317 | 42-5110-006-18 | 42-5110-006-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
34 | 00889024233300 | 42-5110-006-16 | 42-5110-006-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
35 | 00889024233294 | 42-5110-006-14 | 42-5110-006-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
36 | 00889024233287 | 42-5110-006-13 | 42-5110-006-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
37 | 00889024233270 | 42-5110-006-12 | 42-5110-006-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
38 | 00889024233263 | 42-5110-006-11 | 42-5110-006-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
39 | 00889024233256 | 42-5110-006-10 | 42-5110-006-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
40 | 00889024233249 | 42-5110-005-18 | 42-5110-005-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
41 | 00889024233232 | 42-5110-005-16 | 42-5110-005-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
42 | 00889024233225 | 42-5110-005-14 | 42-5110-005-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
43 | 00889024233218 | 42-5110-005-13 | 42-5110-005-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
44 | 00889024233201 | 42-5110-005-12 | 42-5110-005-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
45 | 00889024233195 | 42-5110-005-11 | 42-5110-005-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
46 | 00889024233188 | 42-5110-005-10 | 42-5110-005-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
47 | 00889024233171 | 42-5110-004-18 | 42-5110-004-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
48 | 00889024233164 | 42-5110-004-16 | 42-5110-004-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
49 | 00889024233157 | 42-5110-004-14 | 42-5110-004-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
50 | 00889024233140 | 42-5110-004-13 | 42-5110-004-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00810012483551 | OL45DBS | Drill bit AO QC 4.5 x 145/120mm, Sterile | BIOPRO, INC. | ||
2 | 00810012483544 | OL35DBSL | Drill bit AO QC 3.5 x 195mm, Sterile | BIOPRO, INC. | ||
3 | 00810012483537 | OL35DBS | Drill bit AO QC 3.5 x 110/85mm, Sterile | BIOPRO, INC. | ||
4 | 00810012483520 | OL32DBS | Drill bit AO QC 3.2 x 145/120mm, Sterile | BIOPRO, INC. | ||
5 | 00810012483490 | OL28DBS | Drill bit AO QC 2.8 x 110/85mm, Sterile | BIOPRO, INC. | ||
6 | 00810012483469 | OL25DBS | Drill bit AO QC 2.5 x 110/85mm, Sterile | BIOPRO, INC. | ||
7 | 00810012483407 | OL20DBS | Drill bit AO QC 2.0 x 100/75mm, Sterile | BIOPRO, INC. | ||
8 | 00810012483377 | OL15DBS | Drill bit AO QC 1.5 x 85/60mm, Sterile | BIOPRO, INC. | ||
9 | 00810012483230 | OL11DBS | Drill bit AO QC 1.1 x 85/60mm, Sterile | BIOPRO, INC. | ||
10 | 00810012481922 | 19236 | CANNULATED DRILL STERILE 4.04.5MM | BIOPRO, INC. | ||
11 | 00810012481915 | 19235 | CANNULATED DRILL STERILE 3.03.5MM | BIOPRO, INC. | ||
12 | 00810012481908 | 19234 | CANNULATED DRILL STERILE 2.02.5MM | BIOPRO, INC. | ||
13 | 00810005668743 | CSRW-1000T-405 | Drill 4.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 4.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
14 | 00810005668446 | HAM-1001T-DR45 | Drill 4.5mm diameter cannulated instrument. The Vector Hammertoe Correction Sys Drill 4.5mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. | Vector | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
15 | 00810005666589 | HAM-1001T-DR40 | Drill 4.0mm diameter cannulated instrument. The Vector Hammertoe Correction Sys Drill 4.0mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. | Vector | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
16 | 00810005666572 | HAM-1001T-DR35 | Drill 3.5mm diameter cannulated instrument. The Vector Hammertoe Correction Sys Drill 3.5mm diameter cannulated instrument. The Vector Hammertoe Correction System is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe, and mallet toe. | Vector | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
17 | 00810005665346 | STK-1000T-011 | Instrument: 2.5mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 2.5mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. | Vertex | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
18 | 00810005665339 | STK-1000T-010 | Instrument: 2.3mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 2.3mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. | Vertex | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
19 | 00810005665322 | STK-1000T-009 | Instrument: 2.1mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 2.1mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. | Vertex | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
20 | 00810005665315 | STK-1000T-008 | Instrument: 1.9mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 1.9mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. | Vertex | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
21 | 00810005665308 | STK-1000T-007 | Instrument: 1.7mm Drill. The Vertex Nitinol Staple System consists of a series Instrument: 1.7mm Drill. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating. | Vertex | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
22 | 00810005662727 | CSRW-1000T-404 | Drill 4.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 4.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
23 | 00810005662697 | CSRW-1000T-403 | Drill 3.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 3.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
24 | 00810005662581 | TB-1000T-DR30 | Instrument: Drill for 3.0mm Screw. The Javelin Tailor’s Bunion Fixation System Instrument: Drill for 3.0mm Screw. The Javelin Tailor’s Bunion Fixation System is a single-use bone fixation device intended to be permanently implanted. The system consists of a titanium alloy plate and screws that provide fixation for the 5th metatarsal. | Javelin | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
25 | 00810005662574 | TB-1000T-DR24 | Instrument: Drill for 2.4mm Screw. The Javelin Tailor’s Bunion Fixation System Instrument: Drill for 2.4mm Screw. The Javelin Tailor’s Bunion Fixation System is a single-use bone fixation device intended to be permanently implanted. The system consists of a titanium alloy plate and screws that provide fixation for the 5th metatarsal. | Javelin | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
26 | 00810005662468 | CSRW-1000T-402 | Drill 3.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 3.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
27 | 00810005662437 | CSRW-1000T-401 | Drill 2.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 2.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
28 | 00810005662413 | CSRW-1000T-400S | Solid Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bon Solid Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
29 | 00810005662406 | CSRW-1000T-400 | Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Frac Drill 2.0. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine. | Healix | NVISION BIOMEDICAL TECHNOLOGIES, INC. | |
30 | 00810004729001 | ASY-00491 | ASY-00491 | 7.5 mm Disc Drill, FH7 | NA | INTEGRITY IMPLANTS INC. |
31 | 00810004723146 | ASY-00237 | ASY-00237 | 5.0mm Cortical Drill | NA | INTEGRITY IMPLANTS INC. |
32 | 00810004723139 | ASY-00236 | ASY-00236 | 4.5mm Cortical Drill | NA | INTEGRITY IMPLANTS INC. |
33 | 00810004723122 | ASY-00235 | ASY-00235 | 4.0mm Cortical Drill | NA | INTEGRITY IMPLANTS INC. |
34 | 00810004723115 | ASY-00234 | ASY-00234 | 3.5mm Cortical Drill | NA | INTEGRITY IMPLANTS INC. |
35 | 00810004722026 | ASY-00145 | ASY-00145 | 6.5mm Disc Drill | NA | INTEGRITY IMPLANTS INC. |
36 | 00763000552497 | 981000032 | DRILL 981000032 DRILL | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
37 | 00763000369705 | EX1119037 | DRILL BIT EX1119037 12MM | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
38 | 00763000239879 | EX0119008 | DRILL BIT EX0119008 2.4MM FLUTE LESS | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
39 | 00763000201944 | EX0918010 | DRILL BIT EX0918010 SHORT 11MM | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
40 | 00763000152727 | 6975150 | DRILL BIT 6975150 FLUTELESS DRILL BIT | N/A | MEDTRONIC SOFAMOR DANEK, INC. | |
41 | 00763000140250 | 5580164 | TEMPLATE 5580164 ROD CURVE 5.5/6.0 | NA | MEDTRONIC SOFAMOR DANEK, INC. | |
42 | 00763000140205 | 5580154 | TEMPLATE 5580154 ROD CURVE 4.75 | na | MEDTRONIC SOFAMOR DANEK, INC. | |
43 | 00763000078980 | EX0817017 | RETRACTOR EX0817017 BIOPSY DRILL | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
44 | 00763000078959 | EX0817014 | DRILL EX0817014 BIOPSY CENTER | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
45 | 00763000078935 | EX0817012 | DRILL EX0817012 CENTER | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
46 | 00721902725395 | X0103009 | ZEP DRILL BIT-TRI FLAT-300SS | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
47 | 00721902725364 | X0103007 | ZEP MONO DRILL GUIDE-300SS | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
48 | 00721902725357 | X0103006 | ZEP DUAL DRILL GUIDE-300SS | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
49 | 00721902566509 | X0702636 | CIRCULAR, 13MM DRILL BIT | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | |
50 | 00721902566493 | X0702626 | CIRCULAR ADJUSTABLE DRILL BIT | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. |