Other products from "INNOVASIS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M711CRT006ST0 CRT006ST CP Ti GWO Plate, Cranioplasty, Preformed, Alterable 2 Neuro & Craniofacial Fixation System
2 M711E20024 E2002 E2002 KWQ,KWP,MNH,MNI,NKB Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease Excella II®
3 M711BTA1190 BTA-119 Al, SST, Nylon, Silicone LXH Orthopedic Manual Surgical Instrument 1 PSO
4 M711X212163200 X21216320 X21216320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
5 M711X212163000 X21216300 X21216300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
6 M711X212162800 X21216280 X21216280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
7 M711X212153200 X21215320 X21215320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
8 M711X212153000 X21215300 X21215300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
9 M711X212152800 X21215280 X21215280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
10 M711X212143200 X21214320 X21214320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
11 M711X212143000 X21214300 X21214300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
12 M711X212142800 X21214280 X21214280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
13 M711X212133200 X21213320 X21213320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
14 M711X212133000 X21213300 X21213300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
15 M711X212132800 X21213280 X21213280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
16 M711X212123200 X21212320 X21212320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
17 M711X212123000 X21212300 X21212300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
18 M711X212122800 X21212280 X21212280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
19 M711X212113200 X21211320 X21211320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
20 M711X212113000 X21211300 X21211300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
21 M711X212112800 X21211280 X21211280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
22 M711X212103200 X21210320 X21210320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
23 M711X212103000 X21210300 X21210300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
24 M711X212102800 X21210280 X21210280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
25 M711X212093200 X21209320 X21209320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
26 M711X212093000 X21209300 X21209300 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
27 M711X212092800 X21209280 X21209280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
28 M711X212082800 X21208280 X21208280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
29 M711X210162550 X21016255 X21016255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
30 M711X210162500 X21016250 X21016250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
31 M711X210162250 X21016225 X21016225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
32 M711X210162200 X21016220 X21016220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
33 M711X210153200 X21015320 X21015320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
34 M711X210152800 X21015280 X21015280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
35 M711X210152550 X21015255 X21015255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
36 M711X210152500 X21015250 X21015250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
37 M711X210152250 X21015225 X21015225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
38 M711X210152200 X21015220 X21015220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
39 M711X210143200 X21014320 X21014320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
40 M711X210142800 X21014280 X21014280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
41 M711X210142550 X21014255 X21014255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
42 M711X210142500 X21014250 X21014250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
43 M711X210142250 X21014225 X21014225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
44 M711X210142200 X21014220 X21014220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
45 M711X210133200 X21013320 X21013320 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
46 M711X210132800 X21013280 X21013280 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
47 M711X210132550 X21013255 X21013255 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
48 M711X210132500 X21013250 X21013250 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
49 M711X210132250 X21013225 X21013225 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
50 M711X210132200 X21013220 X21013220 PEEK, Ta MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Px™
Other products with the same Product Code "LXH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00888118119445 99-584-24-01 BLADE KLS-MARTIN L.P.
2 00888118116239 99-584-24-02 BLADE KLS-MARTIN L.P.
3 00888118114389 38-709-07-07 BLADE KLS-MARTIN L.P.
4 00888118114372 38-709-06-07 BLADE KLS-MARTIN L.P.
5 00888118109170 23-656-00-07 PASSER KLS-MARTIN L.P.
6 00888118107534 26-975-03-07 LEVEL ONE KLS-MARTIN L.P.
7 00888118106063 24-015-67-71 LEVEL ONE, STERILE KLS-MARTIN L.P.
8 00888118104502 51-401-93-71 TROCAR TIP, FOR ACT ARM DISTRACTION, INTERNAL, STERILE KLS-MARTIN L.P.
9 00888118095756 26-159-23-07 LEVEL ONE KLS-MARTIN L.P.
10 00888118095749 26-159-20-07 LEVEL ONE KLS-MARTIN L.P.
11 00888118095732 26-159-15-07 LEVEL ONE KLS-MARTIN L.P.
12 00888118080769 51-401-93-09 TROCAR TIP, FOR ACT ARM DISTRACTION, INTERNAL KLS-MARTIN L.P.
13 00888118074973 50-317-10-07 LEVEL ONE TRANSBUCCAL KLS-MARTIN L.P.
14 00888118074935 50-315-00-04 LEVEL ONE KLS-MARTIN L.P.
15 00888118063274 38-709-03-07 REDUCTION INSTRUMENT KLS-MARTIN L.P.
16 00888118063267 38-708-03-07 BLADE KLS-MARTIN L.P.
17 00888118063243 38-708-00-07 REDUCTION INSTRUMENT KLS-MARTIN L.P.
18 00888118061461 38-040-08-07 CARRIER KLS-MARTIN L.P.
19 00888118061454 38-040-06-07 CARRIER KLS-MARTIN L.P.
20 00888118061447 38-040-04-07 CARRIER KLS-MARTIN L.P.
21 00888118061430 38-040-02-07 CARRIER KLS-MARTIN L.P.
22 00888118061386 38-032-10-07 TREPHINE KLS-MARTIN L.P.
23 00888118061379 38-032-05-07 TREPHINE KLS-MARTIN L.P.
24 00888118061324 38-018-01-07 CRUSHER KLS-MARTIN L.P.
25 00888118060266 37-654-00-07 GRID KLS-MARTIN L.P.
26 00888118060259 37-653-00-07 CRUSHER KLS-MARTIN L.P.
27 00888118060242 37-652-00-07 CRUSHER KLS-MARTIN L.P.
28 00888118054272 26-975-06-07 LEVEL ONE KLS-MARTIN L.P.
29 00888118053121 26-155-24-07 LEVEL ONE KLS-MARTIN L.P.
30 00888118053107 26-155-21-07 LEVEL ONE KLS-MARTIN L.P.
31 00888118053091 26-155-20-07 LEVEL ONE KLS-MARTIN L.P.
32 00888118053084 26-155-16-07 LEVEL ONE KLS-MARTIN L.P.
33 00888118053077 26-155-15-07 LEVEL ONE KLS-MARTIN L.P.
34 00888118053060 26-154-24-07 LEVEL ONE KLS-MARTIN L.P.
35 00888118053053 26-154-23-07 LEVEL ONE KLS-MARTIN L.P.
36 00888118053022 26-154-16-07 LEVEL ONE KLS-MARTIN L.P.
37 00888118053015 26-154-15-07 LEVEL ONE KLS-MARTIN L.P.
38 00888118040534 25-438-35-07 LEVEL ONE KLS-MARTIN L.P.
39 00888118026095 22-130-14-07 REAMER KLS-MARTIN L.P.
40 00888118010681 09-040-02-07 CONDENSER KLS-MARTIN L.P.
41 00887919932147 5029503M0 BR9505-02-303 3.2 X 67 MM PINS Brasseler USA Surgical Power & Accessories PETER BRASSELER HOLDINGS, LLC
42 00887919932116 5029502M0 BR9505-02-302 3.2 X 76.2MM PINS Brasseler USA Surgical Power & Accessories PETER BRASSELER HOLDINGS, LLC
43 00887919932086 5029501M0 BR2544-00-111 3.2 X 67 MM PINS Brasseler USA Surgical Power & Accessories PETER BRASSELER HOLDINGS, LLC
44 00887868556647 903720 903720 Guide Pin BIOMET ORTHOPEDICS, LLC
45 00887868551161 42-5399-017-10 42-5399-017-10 Persona® Partial Knee System ZIMMER, INC.
46 00887868550829 42-5399-050-07 42-5399-050-07 Persona® The Personalized Knee System ZIMMER, INC.
47 00887868550812 00-8790-010-30 00-8790-010-30 Continuum®, Trilogy® IT, Allofit® IT ZIMMER, INC.
48 00887868550805 00-7808-035-02 00-7808-035-02 Rasp Handle ZIMMER, INC.
49 00887868550799 00-7808-035-01 00-7808-035-01 Rasp Handle ZIMMER, INC.
50 00887868550782 00-7806-050-00 00-7806-050-00 Zimmer® MIS Hip Instrumentation ZIMMER, INC.