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Vital™ Spinal Fixation System

FDA UDI

Class II (US FDA UDI)

by Highridge Medical, LLC

Identity

Trade Name
Vital™ Spinal Fixation System FDA UDI
Generic Name
Bone-screw internal spinal fixation system rod FDA UDI
Device Name
Z-Rod, Ø5.5 x 450mm, Ti Alloy FDA UDI
Model / Reference
727M1450 FDA UDI
Description
Z-Rod, Ø5.5 x 450mm, Ti Alloy FDA UDI

Identifiers

Catalog Number
727M1450 FDA UDI
Primary DI / UDI-DI
03662663063166 FDA UDI
510(k) Number
K230116 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Bone-screw internal spinal fixation system rod 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

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

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 rod

Vital™ Spinal Fixation System by Highridge Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system rod.

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 ab99bba3-4b48-42a5-8c32-2847edec23f9 36 fields · synced May 29, 2026