Valencia Pedicle Screw System

FDA UDI

Class II (US FDA UDI)

by Altus Spine

Identity

Trade Name: Valencia Pedicle Screw System FDA UDI
Generic Name: Spinal bone set screw FDA UDI
Device Name: T20 Locking Cap FDA UDI
Model / Reference: 915-1520 FDA UDI
Description: T20 Locking Cap FDA UDI

Identifiers

Primary DI / UDI-DI: B41791515201 FDA UDI
FDA Product Code: KWQ FDA UDI
KWP FDA UDI
MNH FDA UDI
NKB FDA UDI
MNI FDA UDI
GMDN Term: Spinal bone set screw FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3060 FDA UDI
888.3050 FDA UDI
888.3070 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Valencia Pedicle Screw System by Altus Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Altus Spine

Sources (1)

FDA UDI 8fc91a9d-b43c-4278-98dd-4da85bd86a46 35 fields · synced Jun 1, 2026