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Jet-X Central

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Jet-X Central FDA UDI
Generic Name
External orthopaedic fixation system, single-use FDA UDI
Device Name
JETX CENTRAL SHORT COMPRESSION/DISTRACTION MODULE FDA UDI
Model / Reference
71051051 FDA UDI
Description
JETX CENTRAL SHORT COMPRESSION/DISTRACTION MODULE FDA UDI

Identifiers

Catalog Number
71051051 FDA UDI
Primary DI / UDI-DI
03596010486455 FDA UDI
510(k) Number
K120871 FDA UDI
FDA Product Code
JDW FDA UDI
GMDN Term
External orthopaedic fixation system, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
Not 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

Jet-X Central by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K120871 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 11d36e46-c28f-4284-a24b-55f38e90a988 37 fields · synced Jun 8, 2026