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Djo Surgical

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
FOUNDATION FEMUR, NONPOROUS, TiNbN COATED, SZ 2, LEFT FDA UDI
Model / Reference
201-08-102 FDA UDI
Description
FOUNDATION FEMUR, NONPOROUS, TiNbN COATED, SZ 2, LEFT FDA UDI

Identifiers

Primary DI / UDI-DI
00888912109253 FDA UDI
510(k) Number
K122239 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Djo Surgical by Djo, Llc — 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

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 83e44838-5aa7-4c73-a7e2-75dc8161bc05 34 fields · synced May 30, 2026