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Synergy

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
SYNERGY FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
SYNERGY FULLY TOOTHED BROACH SIZE 14 SHORT FDA UDI
Model / Reference
71932266 FDA UDI
Description
SYNERGY FULLY TOOTHED BROACH SIZE 14 SHORT FDA UDI

Identifiers

Catalog Number
71932266 FDA UDI
Primary DI / UDI-DI
00885556146200 FDA UDI
510(k) Number
K963509 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Category: Coated hip femur prosthesis, modular

Synergy 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 0954c907-1f26-4f97-8c45-6d3997165ae2 36 fields · synced Jun 8, 2026