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Sl-Plus/Integration-Plus

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
SL-PLUS/INTEGRATION-PLUS FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
SL-PLUS MIA STEM LATERAL NON-CEMENTED WITH TI/HA 3 FDA UDI
Model / Reference
75000188 FDA UDI
Description
SL-PLUS MIA STEM LATERAL NON-CEMENTED WITH TI/HA 3 FDA UDI

Identifiers

Catalog Number
75000188 FDA UDI
Primary DI / UDI-DI
07611996092905 FDA UDI
510(k) Number
K122296 FDA UDI
K143096 FDA UDI
FDA Product Code
KWY FDA UDI
LZO FDA UDI
LWJ FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 FDA UDI
888.3353 FDA UDI
888.3360 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: Coated hip femur prosthesis, modular

Sl-Plus/Integration-Plus by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated 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 5c5d4722-0807-4106-9a92-bb21b70f7549 36 fields · synced Jun 8, 2026