Other products from "COLORADO THERAPEUTICS LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00860002305110 XI-S+ XI1116B-S+ OXK,FTM Mesh, Surgical, Collagen, Large Abdominal Wall Defects,Mesh, Surgical 2 Colorado Therapeutics Xenograft Implant
2 00868623000360 XI-S+ XI0404-S+ FTM,OXK Mesh, Surgical,Mesh, Surgical, Collagen, Large Abdominal Wall Defects 2 Colorado Therapeutics Xenograft Implant
3 00868623000353 XI-S+ XI0203-S+ FTM,OXK Mesh, Surgical,Mesh, Surgical, Collagen, Large Abdominal Wall Defects 2 Colorado Therapeutics Xenograft Implant
4 00868623000346 XI-S+ XI0710-S+ FTM,OXK Mesh, Surgical,Mesh, Surgical, Collagen, Large Abdominal Wall Defects 2 Colorado Therapeutics Xenograft Implant
5 00868623000339 XI-S+ XI0808-S+ FTM,OXK Mesh, Surgical,Mesh, Surgical, Collagen, Large Abdominal Wall Defects 2 Colorado Therapeutics Xenograft Implant
6 00868623000322 XI-S+ XI0508-S+ FTM,OXK Mesh, Surgical,Mesh, Surgical, Collagen, Large Abdominal Wall Defects 2 Colorado Therapeutics Xenograft Implant
7 00868623000315 XI-S+ XI0615-S+ OXK,FTM Mesh, Surgical, Collagen, Large Abdominal Wall Defects,Mesh, Surgical 2 Colorado Therapeutics Xenograft Implant
8 00868623000308 XI-S+ XI0606-S+ FTM,OXK Mesh, Surgical,Mesh, Surgical, Collagen, Large Abdominal Wall Defects 2 Colorado Therapeutics Xenograft Implant
9 00860002305134 XI-S+ XI1014B-S+ OXK,FTM Mesh, Surgical, Collagen, Large Abdominal Wall Defects,Mesh, Surgical 2 Colorado Therapeutics Xenograft Implant
10 00860002305127 XI-S+ XI1014A-S+ OXK,FTM Mesh, Surgical, Collagen, Large Abdominal Wall Defects,Mesh, Surgical 2 Colorado Therapeutics Xenograft Implant
11 00860002305103 XI-S+ XI1116A-S+ OXK,FTM Mesh, Surgical, Collagen, Large Abdominal Wall Defects,Mesh, Surgical 2 Colorado Therapeutics Xenograft Implant
Other products with the same Product Codes "OXK, FTM"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 03700386922053 EBO101 EBO101 CEMENT RESTRICTOR TORNIER
2 00889024458963 32-5014-56 32-5014-056-00 NA ZIMMER, INC.
3 00889024458956 32-5014-53 32-5014-053-00 NA ZIMMER, INC.
4 00868623000360 XI-S+ XI0404-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
5 00868623000360 XI-S+ XI0404-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
6 00868623000353 XI-S+ XI0203-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
7 00868623000353 XI-S+ XI0203-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
8 00868623000346 XI-S+ XI0710-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
9 00868623000346 XI-S+ XI0710-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
10 00868623000339 XI-S+ XI0808-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
11 00868623000339 XI-S+ XI0808-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
12 00868623000322 XI-S+ XI0508-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
13 00868623000322 XI-S+ XI0508-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
14 00868623000315 XI-S+ XI0615-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
15 00868623000315 XI-S+ XI0615-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
16 00868623000308 XI-S+ XI0606-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
17 00868623000308 XI-S+ XI0606-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
18 00860002305141 XI-S+ XI0909C-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
19 00860002305141 XI-S+ XI0909C-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
20 00860002305134 XI-S+ XI1014B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
21 00860002305134 XI-S+ XI1014B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
22 00860002305127 XI-S+ XI1014A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
23 00860002305127 XI-S+ XI1014A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
24 00860002305110 XI-S+ XI1116B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
25 00860002305110 XI-S+ XI1116B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
26 00860002305103 XI-S+ XI1116A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
27 00860002305103 XI-S+ XI1116A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
28 00859389005119 CMCV-009-XXL The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
29 00859389005072 CMCV-009-XLG The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
30 00859389005065 CMCV-009-LRG The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
31 00859389005034 CMCV-009-MED The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
32 00859389005027 CMCV-009-SML The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
33 00856072005142 R20243-1122P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
34 00857072005057 BLM-100-01-1020 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
35 00857072005040 BLM-100-01-1016 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
36 00857072005033 BLM-100-01-0816 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
37 00857072005026 BLM-100-01-1010 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
38 00857072005019 BLM-100-01-0808 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
39 00857072005002 BLM-100-01-0608 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
40 00856072005289 R20252-1020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
41 00856072005197 R20253-1122G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
42 00856072005135 R20243-1018P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
43 00856072005111 R20153-2020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
44 00856072005104 R20153-1620G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
45 00856072005074 R20143-2020P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
46 00856072005043 R20143-0416P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
47 00856072005036 R20252-1122G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
48 00856072005029 R20252-0815G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
49 00856072005012 R20152-2020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
50 00856072005005 R20152-1620G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.