Other products from "GENESYS ORTHOPEDICS SYSTEMS LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M719GU1000 1 GU100 Lumbar Interbody Inserter MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
2 M719GPH418M0 1 GPH1418-M 14mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
3 M719GPH2030S0 1 GPH2030-S 20mm x 30 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
4 M719GPH2030M0 1 GPH2030-M 20mm x 30 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
5 M719GPH2030L0 1 GPH2030-L 20mm x 30 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
6 M719GPH2024S0 1 GPH2024-S 20mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
7 M719GPH2024M0 1 GPH2024-M 20mm x 24 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
8 M719GPH2024L0 1 GPH2024-L 20mm x 24 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
9 M719GPH2018S0 1 GPH2018-S 20mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
10 M719GPH2018M0 1 GPH2018-M 20mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
11 M719GPH2018L0 1 GPH2018-L 20mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
12 M719GPH1830S0 1 GPH1830-S 18mm x 30 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
13 M719GPH1830M0 1 GPH1830-M 18mm x 30 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
14 M719GPH1824S0 1 GPH1824-S 18mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
15 M719GPH1824M0 1 GPH1824-M 18mm x 24 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
16 M719GPH1824L0 1 GPH1824-L 18mm x 24 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
17 M719GPH1818S0 1 GPH1818-S 18mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
18 M719GPH1818M0 1 GPH1818-M 18mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
19 M719GPH1818L0 1 GPH1818-L 18mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
20 M719GPH1630S0 1 GPH1630-S 16mm x 30 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
21 M719GPH1624S0 1 GPH1624-S 16mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
22 M719GPH1624M0 1 GPH1624-M 16mm x 24 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
23 M719GPH1618S0 1 GPH1618-S 16mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
24 M719GPH1618M0 1 GPH1618-M 16mm x 18 degree Hyperlordotic Medium ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
25 M719GPH1618L0 1 GPH1618-L 16mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
26 M719GPH1424S0 1 GPH1424-S 14mm x 24 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
27 M719GPH1418S0 1 GPH1418-S 14mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
28 M719GPH1418L0 1 GPH1418-L 14mm x 18 degree Hyperlordotic Large ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
29 M719GPH1218S0 1 GPH1218-S 12mm x 18 degree Hyperlordotic Small ALIF Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
30 M719GP8010 1 GP801 Lateral Rasp MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
31 M719GP8000 1 GP800 Lateral Trial MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
32 M719GP5360 1 GP536 Large Angled ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
33 M719GP5350 1 GP535 Large Straight ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
34 M719GP5340 1 GP534 Small Angled ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
35 M719GP5330 1 GP533 Small Straight ALIF Curette HTF Curette 1 3DP Lumbar Interbody System
36 M719GP53240 1 GP532-4 12in 4mm Pituitary Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
37 M719GP53220 1 GP532-2 12in 2mm Pituitary Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
38 M719GP53160 1 GP531-6 16in 6mm Kerrison Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
39 M719GP53140 1 GP531-4 16in 4mm Kerrison Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
40 M719GP5300 1 GP530 Toothless Double Action Rongeur HTX Rongeur 1 3DP Lumbar Interbody System
41 M719GP526180 1 GP526-18 18mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
42 M719GP526160 1 GP526-16 16mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
43 M719GP526140 1 GP526-14 14mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
44 M719GP526120 1 GP526-12 12mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
45 M719GP526100 1 GP526-10 10mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
46 M719GP526080 1 GP526-08 8mm ALIF Stick Distractor MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
47 M719GP3D15360 1 GP3D-1536 15mm x 36mm Parallel 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
48 M719GP3D15340 1 GP3D-1534 15mm x 34mm Parallel 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
49 M719GP3D15320 1 GP3D-1532 15mm x 32mm Parallel 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
50 M719GP3D1530C0 1 GP3D-1530C 15mm x 30mm Convex 3DP TPLIF MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 3DP Lumbar Interbody System
Other products with the same Product Codes "KWQ, KWP, NKB"
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