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Ilizarov Systems

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
ILIZAROV SYSTEMS FDA UDI
Generic Name
Cannulated surgical drill guiding pin FDA UDI
Device Name
ILIZAROV DRILL TIP WIRE WITH STOPPER 1.8MM X 400MM FDA UDI
Model / Reference
71070373 FDA UDI
Description
ILIZAROV DRILL TIP WIRE WITH STOPPER 1.8MM X 400MM FDA UDI

Identifiers

Catalog Number
71070373 FDA UDI
Primary DI / UDI-DI
00885556119167 FDA UDI
510(k) Number
K093047 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Cannulated surgical drill guiding pin 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cannulated surgical drill guiding pin

Ilizarov Systems by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated surgical drill guiding pin.

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 1ca66924-e696-4a86-93ba-3c623a7a216a 36 fields · synced Jun 8, 2026