CannCompScrew 1.7mm (Classic)

FDA UDI

Class II (US FDA UDI)

by Trimed, INC.

Identity

Trade Name: CannCompScrew 1.7mm (Classic) FDA UDI
Generic Name: Orthopaedic bone screw (non-sliding) FDA UDI
Device Name: Cannulated Comprs Screw 1.7, 09mm FDA UDI
Model / Reference: C1709 FDA UDI
Description: Cannulated Comprs Screw 1.7, 09mm FDA UDI

Identifiers

Catalog Number: C1709 FDA UDI
Primary DI / UDI-DI: 00842188101847 FDA UDI
510(k) Number: K050681 FDA UDI
FDA Product Code: HWC FDA UDI
GMDN Term: Orthopaedic bone screw (non-sliding) 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

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

Category: Orthopaedic bone screw (non-sliding)

Discover the Cannulated Comprs Screw 1.7mm (Classic), a high-quality, orthopaedic implantable rod designed for internal fixation of limb bones, ribs, sternum, and pelvis in orthopedic surgeries. This screw is ideal for intramedullary fixation/arthrodesis and provides direct interfragmentary stabilization of fractured bones.

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

EVOS — Smith & Nephew, Inc. · Class II
TriLeap Lower Extremity Anatomic Plating System — CROSSROADS EXTREMITY SYSTEMS LLC · Class II
Arthrex® — Arthrex, Inc. · Class II
Zavation — ZAVATION · Class II
STARDRIVE — Synthes GmbH · Class IIb
Arthrex® — Arthrex, Inc. · Class II
Cancellous Screw, Locking — I.T.S. GmbH · Class II
PANGEA — Stryker Corp. · Class II

Cleared under the same submission

K050681 also covers:

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: Trimed, INC.

Sources (1)

FDA UDI 8a06aac0-273c-4ec7-ba97-f5dfc361e280 36 fields · synced Jul 22, 2026