Other products from "NUVASIVE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00887517399779 6942044 CoRoent® XLR, 20x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
2 00887517399700 6941844 CoRoent® XLR, 18x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
3 00887517399335 6941644 CoRoent® XLR, 16x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
4 00887517398765 6941444 CoRoent® XLR, 14x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
5 00887517398499 6941244 CoRoent® XLR, 12x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
6 00887517398420 6941044 CoRoent® XLR, 10x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
7 00887517398055 6932088 CoRoent® XLR, 20x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
8 00887517397683 6931888 CoRoent® XLR, 18x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
9 00887517397256 6931688 CoRoent® XLR, 16x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
10 00887517396822 6931488 CoRoent® XLR, 14x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
11 00887517396457 6931288 CoRoent® XLR, 12x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
12 00887517395641 6922088 CoRoent® XLR, 20x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
13 00887517395634 6922044 CoRoent® XLR, 20x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
14 00887517395269 6921888 CoRoent® XLR, 18x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
15 00887517395252 6921844 CoRoent® XLR, 18x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
16 00887517394880 6921688 CoRoent® XLR, 16x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
17 00887517394873 6921660 CoRoent® XL Wide, 16x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
18 00887517394866 6921655 CoRoent® XL Wide, 16x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
19 00887517394859 6921650 CoRoent® XL Wide, 16x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
20 00887517394842 6921645 CoRoent® XL Wide, 16x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
21 00887517394835 6921644 CoRoent® XLR, 16x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
22 00887517394569 6921488 CoRoent® XLR, 14x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
23 00887517394552 6921460 CoRoent® XL Wide, 14x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
24 00887517394545 6921455 CoRoent® XL Wide, 14x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
25 00887517394538 6921450 CoRoent® XL Wide, 14x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
26 00887517394521 6921445 CoRoent® XL Wide, 14x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
27 00887517394514 6921444 CoRoent® XLR, 14x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
28 00887517394149 6921288 CoRoent® XLR, 12x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
29 00887517394132 6921260 CoRoent® XL Wide, 12x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
30 00887517394125 6921255 CoRoent® XL Wide, 12x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
31 00887517394118 6921250 CoRoent® XL Wide, 12x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
32 00887517394101 6921245 CoRoent® XL Wide, 12x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
33 00887517393791 6921244 CoRoent® XLR, 12x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
34 00887517393722 6921088 CoRoent® XLR, 10x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
35 00887517393715 6921060 CoRoent® XL Wide, 10x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
36 00887517393708 6921055 CoRoent® XL Wide, 10x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
37 00887517393395 6921050 CoRoent® XL Wide, 10x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
38 00887517393388 6921045 CoRoent® XL Wide, 10x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
39 00887517393371 6921044 CoRoent® XLR, 10x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
40 00887517393333 6920860 CoRoent® XL Wide, 8x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
41 00887517393326 6920855 CoRoent® XL Wide, 8x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
42 00887517393319 6920850 CoRoent® XL Wide, 8x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
43 00887517393302 6920845 CoRoent® XL Wide, 8x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
44 00887517392961 6916860 CoRoent® XL, 16x18x60mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
45 00887517392954 6916855 CoRoent® XL, 16x18x55mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
46 00887517392947 6916850 CoRoent® XL, 16x18x50mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
47 00887517392930 6916845 CoRoent® XL, 16x18x45mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
48 00887517392923 6916840 CoRoent® XL, 16x18x40mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
49 00887517392916 6916260 CoRoent® XL Wide, 16x22x60mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
50 00887517392909 6916255 CoRoent® XL Wide, 16x22x55mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
Other products with the same Product Codes "NKG, KWP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08057432565746 ACP-04T526 ACP SINTEA PLUSTEK SRL
2 08057432565739 ACP-04T525 ACP SINTEA PLUSTEK SRL
3 08057432565678 PLS-49T5300 PLS SINTEA PLUSTEK SRL
4 08057432565661 PLS-49T5200 PLS SINTEA PLUSTEK SRL
5 08057432565654 PLS-49T5140 PLS SINTEA PLUSTEK SRL
6 08057432565647 PLS-49T5130 PLS SINTEA PLUSTEK SRL
7 08057432565630 PLS-48T5140 PLS SINTEA PLUSTEK SRL
8 08057432565623 PLS-48T5130 PLS SINTEA PLUSTEK SRL
9 08057432565616 PLS-48T5090 PLS SINTEA PLUSTEK SRL
10 08057432565609 PLS-48T5085 PLS SINTEA PLUSTEK SRL
11 08057432565593 PLS-48T5080 PLS SINTEA PLUSTEK SRL
12 08057432565586 PLS-48T5075 PLS SINTEA PLUSTEK SRL
13 08057432565579 PLS-48T5070 PLS SINTEA PLUSTEK SRL
14 08057432565562 PLS-48T5065 PLS SINTEA PLUSTEK SRL
15 08057432565555 PLS-48T5060 PLS SINTEA PLUSTEK SRL
16 08057432565548 PLS-48T5055 PLS SINTEA PLUSTEK SRL
17 08057432565531 PLS-48T5050 PLS SINTEA PLUSTEK SRL
18 08057432565524 PLS-48T5045 PLS SINTEA PLUSTEK SRL
19 08057432565517 PLS-48T5040 PLS SINTEA PLUSTEK SRL
20 08057432565500 PLS-48T5035 PLS SINTEA PLUSTEK SRL
21 08057432565494 PLS-48T5030 PLS SINTEA PLUSTEK SRL
22 08057432565487  PLS-48CC8 PLS SINTEA PLUSTEK SRL
23 08057432565470  PLS-48CC6 PLS SINTEA PLUSTEK SRL
24 08057432565463  PLS-48CC5 PLS SINTEA PLUSTEK SRL
25 08057432565456  PLS-48CC4 PLS SINTEA PLUSTEK SRL
26 08057432565449  PLS-48CC3 PLS SINTEA PLUSTEK SRL
27 08057432565432  PLS-48CC2 PLS SINTEA PLUSTEK SRL
28 08057432565425  PLS-48CC1 PLS SINTEA PLUSTEK SRL
29 08057432565418  PLS-47CC4 PLS SINTEA PLUSTEK SRL
30 08057432565401  PLS-47CC3 PLS SINTEA PLUSTEK SRL
31 08057432565395  PLS-47CC2 PLS SINTEA PLUSTEK SRL
32 08057432565388 PLS-760T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
33 08057432565371 PLS-760T57 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
34 08057432565364 PLS-760T56 PLS SINTEA PLUSTEK SRL
35 08057432565357 PLS-760T55 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
36 08057432565340 PLS-760T540 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
37 08057432565333 PLS-755T540 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
38 08057432565326 PLS-660T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
39 08057432565319 PLS-655T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
40 08057432565302 PLS-650T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
41 08057432565296 PLS-645T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
42 08057432565289 PLS-640T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
43 08057432565272 PLS-635T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
44 08057432565265 PLS-630T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
45 08057432565258 PLS-6100T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
46 08057432565241 PLS-6095T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
47 08057432565234 PLS-6090T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
48 08057432565227 PLS-6085T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
49 08057432565210 PLS-6080T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL
50 08057432565203 PLS-6075T58 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI& https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml?pageType=manageDI&pageDataLoaded=false&pageMode=read+only&deviceRecordKey=419548# PLS SINTEA PLUSTEK SRL