Identity
- Trade Name
- Vertiflex™ VIP FDA UDI
- Generic Name
- Lumbar interspinous decompression instrument set, single-use FDA UDI
- Device Name
- Instrument Platform Kit FDA UDI
- Model / Reference
- 140-9800 FDA UDI
- Description
- Instrument Platform Kit FDA UDI
Identifiers
- Catalog Number
- 140-9800 FDA UDI
- Primary DI / UDI-DI
- 00884662000611 FDA UDI
- PMA Number
- P140004 FDA UDI
- FDA Product Code
- NQO FDA UDI
- GMDN Term
- Lumbar interspinous decompression instrument set, single-use FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Category: Lumbar interspinous decompression instrument set, single-use
Vertiflex™ VIP by Boston Scientific Neuromodulation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lumbar interspinous decompression instrument set, single-use.
- TSI — TEDAN SURGICAL INNOVATIONS, L.L.C. · Class II
- Superion™ SUI — Boston Scientific Neuromodulation · Class III
Cleared under the same submission
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 III | Pending data |
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Manufacturer
- Manufacturer
- Boston Scientific Neuromodulation
Sources (1)
- FDA UDI 5737ccae-5598-4727-94bb-667a42d755b8 35 fields · synced May 30, 2026