Primary Device ID | M7391410714090 |
NIH Device Record Key | fe116a01-a779-4c37-ac7b-f3d879f291c6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cervical PEEK Cage-Lordotic 14 x 9mm |
Version Model Number | 14107-1409 |
Company DUNS | 836975784 |
Company Name | CAPTIVA SPINE, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M7391410714090 [Primary] |
ODP | Intervertebral Fusion Device With Bone Graft, Cervical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M7391410714090]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2015-08-28 |
00850065741567 - Trial 7mm | 2025-08-27 7mm Trial |
00850065741574 - Trial 8mm | 2025-08-27 8mm Trial |
00850065741581 - Trial 9mm | 2025-08-27 9mm Trial |
00850065741598 - Trial 10mm | 2025-08-27 10mm Trial |
00850065741604 - Trial 11mm | 2025-08-27 11mm Trial |
00850065741611 - Trial 12mm | 2025-08-27 12mm Trial |
00850065741628 - Distraction Paddle - 7mm | 2025-08-27 Distraction Paddle - 7mm |
00850065741635 - Distraction Paddle - 8mm | 2025-08-27 Distraction Paddle - 8mm |