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OIC Intramedullary Nail System

FDA UDI

Class II (US FDA UDI)

by Orthopaedic Implant Company, The

Identity

Trade Name
OIC Intramedullary Nail System FDA UDI
Generic Name
Bone-nailing spacer FDA UDI
Device Name
STRAIGHT CANNULA FDA UDI
Model / Reference
01-IMSE04 FDA UDI
Description
STRAIGHT CANNULA FDA UDI

Identifiers

Primary DI / UDI-DI
10811998038039 FDA UDI
510(k) Number
K181184 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone-nailing spacer 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

No

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: Bone-nailing spacer

OIC Intramedullary Nail System by Orthopaedic Implant Company, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-nailing spacer.

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 6a6cf5d5-f1a1-454a-abfb-bb342770dfd4 35 fields · synced May 31, 2026