Primary Device ID | 00849777011792 |
NIH Device Record Key | 60d9ca36-8962-4fe3-a841-76a873f1dfb4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Demineralized Bone Matrix, 1cc |
Version Model Number | OM-PUT01P |
Company DUNS | 081224143 |
Company Name | Xtant Medical Holdings, Inc. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | true |
Device Kit | false |
Device Combination Product | true |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
00840311207435 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x25 |
00840311207442 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x30 |
00840311207459 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x35 |
00840311207466 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x40 |
00840311207473 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x45 |
00840311207480 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x50 |
00840311207497 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x55 |
00840311207503 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x60 |