VBOSS 33662005MO
GUDID 04546540389411
LARGE OVAL ENDCAP
Stryker Corporation
Metallic spinal fusion cage, non-sterile| Primary Device ID | 04546540389411 |
| NIH Device Record Key | 78bc6c70-0d96-4a0e-8d44-70ff22c4b3e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VBOSS |
| Version Model Number | 33662005MO |
| Catalog Number | 33662005MO |
| Company DUNS | 149183167 |
| Company Name | Stryker Corporation |
| 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 | 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 |
Device Dimensions
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
| Angle | 5 degree |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540389411 [Primary] |
FDA Product Code
| MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
[04546540389411]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-11-26 |
| Device Publish Date | 2015-09-14 |
On-Brand Devices [VBOSS]
Trademark Results [VBOSS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VBOSS 78339294 2990502 Live/Registered |
STRYKER EUROPEAN HOLDINGS I, LLC 2003-12-11 |
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