Primary Device ID | 10840642106862 |
NIH Device Record Key | 0de0f844-dd1c-41f8-9312-aaf25945f987 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Velocity™ Expandable Interbody System |
Version Model Number | 11-2365 |
Catalog Number | 11-2365 |
Company DUNS | 067789763 |
Company Name | Spine Wave, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
10840642107876 | Velocity® Lateral Surgical Gun Assembly |
10840642107869 | Velocity® Posterior Surgical Gun Assembly |
10840642106916 | Expandable Implant, 25(L) X 10(W) X 8-14(H) 8 Degree Lordotic |
10840642106909 | Expandable Implant, 22(L) X 10(W) X 8-14(H) 8 Degree Lordotic |
10840642106893 | Expandable Implant, 25(L) X 10(W) X 8-14(H), Biconvex |
10840642106886 | Expandable Implant, 22(L) X 10(W) X 8-14(H), Biconvex |
10840642106879 | Expandable Implant, 55(L) X 18(W) X 8-13(H) 10 Degree Lordotic |
10840642106862 | Expandable Implant, 50(L) X 18(W) X 8-13(H) 10 Degree Lordotic |
10840642106848 | Expandable Implant, 55(L) X 18(W) X 8-13(H) Biconvex |
10840642106831 | Expandable Implant, 50(L) X (18)W X 8-13(H) Biconvex |
10840642106824 | Expandable Implant, 45(L) X (18)W X 8-13(H) Biconvex |
10840642106817 | Expandable Implant, 25(L) X 10(W) X 7-12(H), 8 Degree Lordotic |
10840642106800 | Expandable Implant, 22(L) X 10(W) X 7-12(H), 8 Degree Lordotic |
10840642106794 | Expandable Implant, 25(L) X 10(W) X 7-12(H), Biconvex |
10840642106787 | Expandable Implant, 22(L) X 10(W) X 7-12(H), Biconvex |