← Back to catalogue

Echelon

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
ECHELON FDA UDI
Generic Name
Uncoated femoral stem prosthesis, one-piece FDA UDI
Device Name
ECHELON CEMENTED FEMORAL COMPONENT SZ 16 175MM FDA UDI
Model / Reference
71310116 FDA UDI
Description
ECHELON CEMENTED FEMORAL COMPONENT SZ 16 175MM FDA UDI

Identifiers

Catalog Number
71310116 FDA UDI
Primary DI / UDI-DI
03596010328533 FDA UDI
510(k) Number
K963486 FDA UDI
FDA Product Code
LPH FDA UDI
JDI FDA UDI
GMDN Term
Uncoated femoral stem prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
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 femoral stem prosthesis, one-piece

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

Similar devices

Also classified as Uncoated femoral stem prosthesis, one-piece.

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 1ba25efd-94c2-4ebd-ba31-d2f4ec985f78 36 fields · synced Jun 8, 2026