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Contours VPS Volar Plating System

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
Contours VPS Volar Plating System FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
SCREW, DISTAL RADIUS VOLAR, M3.5 X 0.6 MICROTHREAD, 26 MM, TITANIUM FDA UDI
Model / Reference
1 FDA UDI
Description
SCREW, DISTAL RADIUS VOLAR, M3.5 X 0.6 MICROTHREAD, 26 MM, TITANIUM FDA UDI

Identifiers

Catalog Number
PSC2026TCE FDA UDI
Primary DI / UDI-DI
18054242516460 FDA UDI
510(k) Number
K042766 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, non-sterile

Contours VPS Volar Plating System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI d6c70a21-1bbc-4ac5-8ac3-8504bf4a09db 36 fields · synced May 30, 2026