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Simple Locking Intramedullary (slim) System

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Canada ULC

Identity

Trade Name
SIMPLE LOCKING INTRAMEDULLARY (SLIM) SYSTEM FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
SLIM BLANK Ø4.0 x 300mm FDA UDI
Model / Reference
SLM-40-BL3 FDA UDI
Description
SLIM BLANK Ø4.0 x 300mm FDA UDI

Identifiers

Catalog Number
SLM-40-BL3 FDA UDI
Primary DI / UDI-DI
07540194008671 FDA UDI
510(k) Number
K143355 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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 — 4 Millimeter FDA UDI
Length — 300 Millimeter FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

Simple Locking Intramedullary (slim) System by Orthopediatrics Canada ULC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f1579cf8-4ee5-4778-a99c-a2dd005191af 38 fields · synced Jun 6, 2026