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Vu ePOD™

FDA UDI

Class II (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Vu ePOD™ FDA UDI
Generic Name
Vertebral body prosthesis, non-sterile FDA UDI
Device Name
11mm x 30mm Tapered 5 deg FDA UDI
Model / Reference
14-TA-3011 FDA UDI
Description
11mm x 30mm Tapered 5 deg FDA UDI

Identifiers

Catalog Number
14-TA-3011 FDA UDI
Primary DI / UDI-DI
10889981039158 FDA UDI
510(k) Number
K082712 FDA UDI
FDA Product Code
MQP FDA UDI
MAX FDA UDI
GMDN Term
Vertebral body prosthesis, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Vertebral body prosthesis, non-sterile

Vu ePOD™ by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral body prosthesis, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f5709aa7-d30e-42d0-af08-d6620636096a 37 fields · synced Jun 8, 2026