No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00849044083866 | 652.632 | Single Trial, 32mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
2 | 00849044083859 | 652.630 | Single Trial, 30mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
3 | 00849044092882 | 688.400 | Rod Cutter | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
4 | 00849044076011 | 601.405 | Trial, Parallel, 5mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
5 | 00849044072389 | 685.420 | Calipers | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
6 | 00849044056075 | 624.613 | REVERE Power Bender | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
7 | 00849044092875 | 688.368 | Small Plate Caddy | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
8 | 00849044092868 | 688.367 | AP Inserter Caddy | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
9 | 00849044092851 | 688.366 | AP Inserter, 44-55mm Plate | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
10 | 00849044092844 | 688.365 | AP Inserter, 35-41mm Plate | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
11 | 00849044092905 | 688.460 | SP-Fix ARC Plate Pincher | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
12 | 00849044092899 | 688.450 | Plate Pincher | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
13 | 00849044086089 | 671.303 | Screwdriver Sleeve | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
14 | 00849044092837 | 688.351 | Lateral Barrel Inserter, 44-55mm Plate | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
15 | 00849044092820 | 688.350 | Lateral Barrel Inserter, 35-41mm Plate | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
16 | 00849044092813 | 688.331 | Removal Driver | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
17 | 00849044092806 | 688.330 | Hex Key | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
18 | 00849044092790 | 688.320 | Implant Compressor | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
19 | 00849044092783 | 688.315 | Rod Holder | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
20 | 00849044092776 | 688.314 | Barrel Holder | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
21 | 00849044092769 | 688.311 | Plate Holder, 44-55mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
22 | 00849044092752 | 688.310 | Plate Holder, 35-41mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
23 | 00849044092745 | 688.300 | Distractor | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
24 | 00849044092738 | 688.275 | Rod Trial | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
25 | 00849044092721 | 688.255 | Plate Trial, 55mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
26 | 00849044092714 | 688.250 | Plate Trial, 50mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
27 | 00849044092707 | 688.247 | Plate Trial, 47mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
28 | 00849044092691 | 688.244 | Plate Trial, 44mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
29 | 00849044092684 | 688.241 | Plate Trial, 41mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
30 | 00849044092677 | 688.238 | Plate Trial, 38mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
31 | 00849044092660 | 688.235 | Plate Trial, 35mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
32 | 00849044092653 | 688.232 | Plate Trial, 32mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
33 | 00849044092646 | 688.229 | Plate Trial, 29mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
34 | 00849044092615 | 688.170 | LP-Ti Barrel Trial, 20mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
35 | 00849044092608 | 688.168 | LP-Ti Barrel Trial, 18mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
36 | 00849044092592 | 688.166 | LP-Ti Barrel Trial, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
37 | 00849044092585 | 688.164 | LP-Ti Barrel Trial, 14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
38 | 00849044092578 | 688.162 | LP-Ti Barrel Trial, 12mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
39 | 00849044092561 | 688.160 | LP-Ti Barrel Trial, 10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
40 | 00849044092554 | 688.158 | LP-Ti Barrel Trial, 8mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
41 | 00849044092530 | 688.120 | Trial, 20mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
42 | 00849044092523 | 688.118 | Trial, 18mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
43 | 00849044092516 | 688.116 | Trial, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
44 | 00849044092509 | 688.114 | Trial, 14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
45 | 00849044092493 | 688.112 | Trial, 12mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
46 | 00849044092486 | 688.110 | Trial, 10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
47 | 00849044092479 | 688.108 | Trial, 8mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
48 | 00849044092462 | 688.075 | Rasp | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
49 | 00849044092455 | 688.060 | Spinous Process Rake | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
50 | 00849044089837 | 524.885 | 8.5mm REVERE Monoaxial Reduction Screw, 90mm | KWP,MNH,KWQ,NKB,MNI | APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINAL PEDICLE FIXATION | 2 | REVERE |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 28031497000668 | SPC0522 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Hip | TECRES SPA | |
2 | 28031497000651 | SPC0422 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Hip | TECRES SPA | |
3 | 28031497000644 | SPC0322 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Hip | TECRES SPA | |
4 | 28031497000637 | SPC0222 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Hip | TECRES SPA | |
5 | 28031497000620 | SPC0122 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Hip | TECRES SPA | |
6 | 28031497000613 | SPC0022 | Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cementcoated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Hip | TECRES SPA | |
7 | 17613327311089 | I-H1236HA00 | I-H1236HA00 | SPECIALTY TRIDENT TRIAL CONTAINMENT SCREW-LONGER | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
8 | 17613327261100 | 0937-8-205 | 0937-8-205 | EXETER MIS HALF MOON FEMORAL CEMENT SEAL | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
9 | 17613327141358 | 0937-3-215 | 0937-3-215 | EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
10 | 17613327141310 | 0937-3-225 | 0937-3-225 | EXETER MIS HORSE COLLAR FEMORAL CEMENT SEAL | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
11 | 10885862536174 | 01-003-04-0009 | 01-003-04-0009 | CALCAR PLANER BLADE 1" | NA | EXACTECH, INC. |
12 | 10885862535894 | 01-003-04-0008 | 01-003-04-0008 | CALCAR PLANER BLADE 1.3" | NA | EXACTECH, INC. |
13 | 10885862534088 | 01-003-06-0008 | 01-003-06-0008 | CANAL FINDER, TOOTHED STARTER BROACH | NA | EXACTECH, INC. |
14 | 10885862530103 | 01-003-02-0007 | 01-003-02-0007 | DUAL OFFSET BROACH HANDLE, RIGHT, NO TWIST | NA | EXACTECH, INC. |
15 | 10885862530097 | 01-003-02-0006 | 01-003-02-0006 | DUAL OFFSET BROACH HANDLE, LEFT, NO TWIST | NA | EXACTECH, INC. |
16 | 10885862528490 | 190-61-15 | 190-61-15 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
17 | 10885862528483 | 190-61-14 | 190-61-14 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
18 | 10885862528476 | 190-61-13 | 190-61-13 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
19 | 10885862528469 | 190-61-11 | 190-61-11 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
20 | 10885862528452 | 190-61-09 | 190-61-09 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
21 | 10885862528445 | 190-61-07 | 190-61-07 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
22 | 10885862528438 | 190-61-05 | 190-61-05 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
23 | 10885862528421 | 190-60-15 | 190-60-15 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
24 | 10885862528414 | 190-60-14 | 190-60-14 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
25 | 10885862528407 | 190-60-13 | 190-60-13 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
26 | 10885862528391 | 190-60-11 | 190-60-11 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
27 | 10885862528384 | 190-60-09 | 190-60-09 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
28 | 10885862528377 | 190-60-07 | 190-60-07 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
29 | 10885862528360 | 190-60-05 | 190-60-05 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
30 | 10885862527028 | 190-61-12 | 190-61-12 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
31 | 10885862527011 | 190-61-10 | 190-61-10 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
32 | 10885862527004 | 190-61-08 | 190-61-08 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
33 | 10885862526991 | 190-61-06 | 190-61-06 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
34 | 10885862526984 | 190-61-04 | 190-61-04 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
35 | 10885862526977 | 190-60-12 | 190-60-12 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
36 | 10885862526960 | 190-60-10 | 190-60-10 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
37 | 10885862526953 | 190-60-08 | 190-60-08 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
38 | 10885862526946 | 190-60-06 | 190-60-06 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
39 | 10885862526939 | 190-60-04 | 190-60-04 | Alteon Highly Polished Femoral Stem | Alteon | EXACTECH, INC. |
40 | 10885862513908 | 191-03-15 | 191-03-15 | ALT HA S COMP BRCH SZ 15 | Alteon | EXACTECH, INC. |
41 | 10885862513892 | 191-03-14 | 191-03-14 | ALT HA S COMP BRCH SZ 14 | Alteon | EXACTECH, INC. |
42 | 10885862513885 | 191-03-13 | 191-03-13 | ALT HA S COMP BRCH SZ 13 | Alteon | EXACTECH, INC. |
43 | 10885862513878 | 191-03-12 | 191-03-12 | ALT HA S COMP BRCH SZ 12 | Alteon | EXACTECH, INC. |
44 | 10885862513861 | 191-03-11 | 191-03-11 | ALT HA S COMP BRCH SZ 11 | Alteon | EXACTECH, INC. |
45 | 10885862513854 | 191-03-10 | 191-03-10 | ALT HA S COMP BRCH SZ 10 | Alteon | EXACTECH, INC. |
46 | 10885862513847 | 191-03-09 | 191-03-09 | ALT HA S COMP BRCH SZ 9 | Alteon | EXACTECH, INC. |
47 | 10885862513830 | 191-03-08 | 191-03-08 | ALT HA S COMP BRCH SZ 8 | Alteon | EXACTECH, INC. |
48 | 10885862513823 | 191-03-07 | 191-03-07 | ALT HA S COMP BRCH SZ 7 | Alteon | EXACTECH, INC. |
49 | 10885862513816 | 191-03-06 | 191-03-06 | ALT HA S COMP BRCH SZ 6 | Alteon | EXACTECH, INC. |
50 | 10885862513809 | 191-03-05 | 191-03-05 | ALT HA S COMP BRCH SZ 5 | Alteon | EXACTECH, INC. |