IVA Cage TIP.36090014
GUDID 08800039827492
IVA TLIF(BULLET) CAGE L36 x W9 x H14
DIOMEDICAL CO.,LTD.
Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable| Primary Device ID | 08800039827492 |
| NIH Device Record Key | 3fa76dd5-f423-4615-92fe-3a6726d987cf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IVA Cage |
| Version Model Number | A |
| Catalog Number | TIP.36090014 |
| Company DUNS | 557795909 |
| Company Name | DIOMEDICAL CO.,LTD. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
Customer Support Contacts
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com | |
| Phone | +82313699470 |
| info@huvexel.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800039827492 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K162220
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
[08800039827492]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-22 |
| Device Publish Date | 2020-07-14 |
On-Brand Devices [IVA Cage]
| 08800039872287 | IVA TLIF(Bullet) CAGE L28xW09xA0xH17 |
| 08800039870573 | TLIF Bullet Type Impactor |
| 08800039870498 | ACIF NC TRIAL L14XW16XA7XH11 |
| 08800039870481 | ACIF NC TRIAL L14XW16XA7XH12 |
| 08800039870467 | ALIF TRIAL L24xW35xA15xH17 |
| 08800039870450 | ALIF TRIAL L24xW35xA15xH15 |
| 08800039870443 | ALIF TRIAL L24xW35xA15xH13 |
| 08800039870436 | ALIF TRIAL L24xW35xA15xH11 |
| 08800039870429 | ALIF TRIAL L24xW35xA15xH9 |
| 08800039870412 | ALIF TRIAL L24xW35xA8xH17 |
| 08800039870405 | ALIF TRIAL L24xW35xA8xH15 |
| 08800039870399 | ALIF TRIAL L24xW35xA8xH13 |
| 08800039870382 | ALIF TRIAL L24xW35xA8xH11 |
| 08800039870375 | ALIF TRIAL L24xW35xA8xH9 |
| 08800039870368 | ALIF TRIAL L22xW29xA15xH17 |
| 08800039870351 | ALIF TRIAL L22xW29xA15xH15 |
| 08800039870344 | ALIF TRIAL L22xW29xA15xH13 |
| 08800039870337 | ALIF TRIAL L22xW29xA15xH11 |
| 08800039870320 | ALIF TRIAL L22xW29xA15xH9 |
| 08800039870313 | ALIF TRIAL L22xW29xA8xH17 |
| 08800039870306 | ALIF TRIAL L22xW29xA8xH15 |
| 08800039870290 | ALIF TRIAL L22xW29xA8xH13 |
| 08800039870283 | ALIF TRIAL L22xW29xA8xH11 |
| 08800039870276 | ALIF TRIAL L22xW29xA8xH9 |
| 08800039842112 | IVA Anterior Lumbar PEEK Straight Type 22*29*15*19 |
| 08800039842105 | IVA Anterior Lumbar PEEK Straight Type 22*29*15*17 |
| 08800039842099 | IVA Anterior Lumbar PEEK Straight Type 22*29*15*15 |
| 08800039842082 | IVA Anterior Lumbar PEEK Straight Type 22*29*15*13 |
| 08800039842075 | IVA Anterior Lumbar PEEK Straight Type 22*29*15*11 |
| 08800039842068 | IVA Anterior Lumbar PEEK Straight Type 22*29*15*09 |
| 08800039842051 | IVA Anterior Lumbar PEEK Straight Type 22*29*08*19 |
| 08800039842044 | IVA Anterior Lumbar PEEK Straight Type 22*29*08*17 |
| 08800039842037 | IVA Anterior Lumbar PEEK Straight Type 22*29*08*15 |
| 08800039842020 | IVA Anterior Lumbar PEEK Straight Type 22*29*08*13 |
| 08800039842013 | IVA Anterior Lumbar PEEK Straight Type 22*29*08*11 |
| 08800039842006 | IVA Anterior Lumbar PEEK Straight Type 22*29*08*09 |
| 08800039834087 | RASP 28X39 H21 |
| 08800039834070 | RASP 28X39 H19 |
| 08800039834063 | RASP 28X39 H17 |
| 08800039834056 | RASP 28X39 H15 |
| 08800039834049 | RASP 28X39 H13 |
| 08800039834032 | RASP 28X39 H11 |
| 08800039834025 | RASP 28X39 H9 |
| 08800039834018 | RASP 24X35 H21 |
| 08800039834001 | RASP 24X35 H19 |
| 08800039833998 | RASP 24X35 H17 |
| 08800039833981 | RASP 24X35 H15 |
| 08800039833974 | RASP 24X35 H13 |
| 08800039833967 | RASP 24X35 H11 |
| 08800039833950 | RASP 24X35 H9 |
Trademark Results [IVA Cage]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 IVA CAGE 88067542 5779230 Live/Registered |
HUVEXEL CO., LTD. 2018-08-07 |
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