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Spectron

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Spectron FDA UDI
Generic Name
Uncoated hip femur prosthesis, modular FDA UDI
Device Name
SPECTRON EF 12/14 TAPER LONG STRAIGHT 165MM LARGE FDA UDI
Model / Reference
71312233 FDA UDI
Description
SPECTRON EF 12/14 TAPER LONG STRAIGHT 165MM LARGE FDA UDI

Identifiers

Catalog Number
71312233 FDA UDI
Primary DI / UDI-DI
03596010386380 FDA UDI
510(k) Number
K970351 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Uncoated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Uncoated hip femur prosthesis, modular

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

Similar devices

Also classified as Uncoated hip femur prosthesis, modular.

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 52b5e04b-91eb-4f1e-9160-55849a465e43 36 fields · synced Jun 8, 2026