Other products from "ZIMMER SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024331891 1875-314 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
2 00889024331884 1875-312 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
3 00889024331877 1875-310 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
4 00889024331860 1875-308 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
5 00889024331853 1875-114 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
6 00889024331846 1875-112 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
7 00889024331839 1875-110 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
8 00889024331822 1875-108 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
9 00889024331815 1874-500 1874-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
10 00889024331808 1874-300 1874-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
11 00889024331792 1874-100 1874-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
12 00889024331785 1873-1 1873-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
13 00889024331778 1872-2 1872-2 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
14 00889024332041 1894-400 1894-400 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
15 00889024331761 1871-1 1871-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
16 00889024331754 1870-1 1870-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
17 00889024331747 1869-1 1869-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
18 00889024331730 1868-14 1868-14 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
19 00889024331723 1868-12 1868-12 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
20 00889024331716 1868-10 1868-10 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
21 00889024331709 1868-08 1868-08 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
22 00889024331693 1865-514 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
23 00889024331686 1865-512 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
24 00889024332058 1894-500 1894-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
25 00889024332034 1894-300 1894-300 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
26 00889024332027 1894-200 1894-200 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
27 00889024332010 1894-100 1894-100 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
28 00889024332003 1879-500 1879-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
29 00889024331990 1879-300 1879-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
30 00889024331983 1879-100 1879-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
31 00889024331976 1877-500 1877-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
32 00889024331969 1877-300 1877-300 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
33 00889024331952 1877-100 1877-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
34 00889024331945 1876-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
35 00889024331938 1875-514 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
36 00889024331921 1875-512 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
37 00889024331914 1875-510 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
38 00889024331907 1875-508 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
39 00889024331679 1865-510 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
40 00889024331662 1865-508 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
41 00889024331655 1865-314 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
42 00889024331648 1865-312 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
43 00889024331631 1865-310 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
44 00889024331624 1865-308 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
45 00889024331617 1865-114 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
46 00889024331600 1865-112 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
47 00889024331594 1865-110 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
48 00889024331587 1865-108 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
49 00889024331563 1859-1 1859-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
50 00889024331556 1857-500 1857-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
Other products with the same Product Codes "KWQ, OSH, KWP, MNH, NKB, MNI"
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