← Back to catalogue

Sl-Plus

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
SL-PLUS FDA UDI
Generic Name
Femoral stem prosthesis trial FDA UDI
Device Name
SL-PLUS DETACHABLE RASP 8 FDA UDI
Model / Reference
75007302 FDA UDI
Description
SL-PLUS DETACHABLE RASP 8 FDA UDI

Identifiers

Catalog Number
75007302 FDA UDI
Primary DI / UDI-DI
07611996074994 FDA UDI
510(k) Number
K123598 FDA UDI
FDA Product Code
JDI FDA UDI
KWY FDA UDI
LWJ FDA UDI
LZO FDA UDI
GMDN Term
Femoral stem prosthesis trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3390 FDA UDI
888.3360 FDA UDI
888.3353 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, manual, reusableFemoral stem prosthesis trial

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

Similar devices

Also classified as Femoral stem prosthesis trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3405fc08-256b-4323-8ce2-76eb6682dbeb 36 fields · synced Jun 8, 2026