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Contours Proximal Humeral Plate (PHP)

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
Contours Proximal Humeral Plate (PHP) FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
MAIN LOCKING SCREW (D. 6.0 MM) L. 40MM STERILE FDA UDI
Model / Reference
1 FDA UDI
Description
MAIN LOCKING SCREW (D. 6.0 MM) L. 40MM STERILE FDA UDI

Identifiers

Catalog Number
99-TP1640 FDA UDI
Primary DI / UDI-DI
18054242510246 FDA UDI
510(k) Number
K122541 FDA UDI
FDA Product Code
KTW FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 40 Millimeter FDA UDI
Outer Diameter — 6.0 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Contours Proximal Humeral Plate (PHP) 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, 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 ea4535af-4bea-42fa-8e5a-3876d433e7ab 37 fields · synced May 31, 2026