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Vital™

FDA UDI

Class II (US FDA UDI)

by Biomet Spine Llc

Identity

Trade Name
Vital™ FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Model / Reference
806M8515 FDA UDI

Identifiers

Catalog Number
806M8515 FDA UDI
Primary DI / UDI-DI
00887868318658 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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: Bone-screw internal spinal fixation system, non-sterile

Discover the latest innovation in orthopedic spinal fixation with the Vital device, a cutting-edge non-sterile implantable system designed to provide immobilization and stabilization of spinal segments. With its unique combination of anchors, interconnection mechanisms, longitudinal members, and transverse connectors, this device offers a robust solution for treating various spinal instabilities or deformities. Learn more about the features, safety, and regulatory compliance of the Vital device.

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Spine Llc

Sources (1)

  • FDA UDI d54109b1-9bd5-42b5-aac3-6b5ce63d5277 35 fields · synced Jul 30, 2026