← Back to catalogue

Vu aPod™ - L

FDA UDI

Class II (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Vu aPod™ - L FDA UDI
Generic Name
Vertebral body prosthesis, non-sterile FDA UDI
Device Name
LATERAL IMPLANT, SPINPLATE™ ANGLED, LORDOTIC, 12mm X 60mm X 12° FDA UDI
Model / Reference
31-14-1260-12 FDA UDI
Description
LATERAL IMPLANT, SPINPLATE™ ANGLED, LORDOTIC, 12mm X 60mm X 12° FDA UDI

Identifiers

Catalog Number
31-14-1260-12 FDA UDI
Primary DI / UDI-DI
10889981046118 FDA UDI
510(k) Number
K112986 FDA UDI
FDA Product Code
MAX FDA UDI
OVD FDA UDI
GMDN Term
Vertebral body prosthesis, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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 aPod™ - L 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6455e97c-9dbe-40be-86f7-f49cd6716b5b 37 fields · synced Jun 8, 2026