Identity
- Trade Name
- iVAS FDA UDI
- Generic Name
- Balloon kyphoplasty kit FDA UDI
- Device Name
- 8 gauge 15mm iVAS Elite Single Balloon Kit FDA UDI
- Model / Reference
- 808815000 FDA UDI
- Description
- 8 gauge 15mm iVAS Elite Single Balloon Kit FDA UDI
Identifiers
- Catalog Number
- 0808-815-000 FDA UDI
- Primary DI / UDI-DI
- 07613327142778 FDA UDI
- FDA Product Code
- NDN FDA UDI
- GMDN Term
- Balloon kyphoplasty kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3027 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 8.0 Gauge FDA UDI
Category: Balloon kyphoplasty kit
iVAS by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Balloon kyphoplasty kit.
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- SYNTH™ PLUS — IMEDICOM CO., LTD. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI fe04c106-f100-41a9-a629-2474cb9a09bd 37 fields · synced May 30, 2026