← Back to catalogue

Liberty Anterior Cervical Plate

FDA UDI

Class II (US FDA UDI)

by Valorus Spine, Llc

Identity

Trade Name
Liberty Anterior Cervical Plate FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Variable Screw, Self Drilling, 4.0x14mm FDA UDI
Model / Reference
20-07-4014 FDA UDI
Description
Variable Screw, Self Drilling, 4.0x14mm FDA UDI

Identifiers

Primary DI / UDI-DI
00811771030901 FDA UDI
510(k) Number
K172585 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Spinal bone screw, non-bioabsorbable

Liberty Anterior Cervical Plate by Valorus Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Cleared under the same submission

K172585 also covers:

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

Manufacturer
Valorus Spine, Llc

Sources (1)

  • FDA UDI d38b0105-0890-4189-934d-a045b793e92c 35 fields · synced May 31, 2026