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Monster Screw System

FDA UDI

Class II (US FDA UDI)

by Paragon 28

Identity

Trade Name
Monster Screw System FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
Mini Monster Headed, Short Thread, 2.0 x 9mm FDA UDI
Model / Reference
P20-120-009S FDA UDI
Description
Mini Monster Headed, Short Thread, 2.0 x 9mm FDA UDI

Identifiers

Catalog Number
P20-120-009S FDA UDI
Primary DI / UDI-DI
00889795001276 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2 Millimeter FDA UDI

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

Monster Screw System by Paragon 28 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI c0ea408f-fab1-4906-9d4d-ee1ffa656424 35 fields · synced May 30, 2026