VerSys®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name: VerSys® FDA UDI
Generic Name: Uncoated hip femur prosthesis, modular FDA UDI
Model / Reference: 7833-15 FDA UDI

Identifiers

Primary DI / UDI-DI: 00889024362192 FDA UDI
510(k) Number: K955473 FDA UDI
FDA Product Code: JDG FDA UDI
KWL FDA UDI
LWJ FDA UDI
JDI FDA UDI
GMDN Term: Uncoated hip femur prosthesis, modular FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3360 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Uncoated hip femur prosthesis, modular

VerSys® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Uncoated hip femur prosthesis, modular.

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S-ROM — DEPUY ORTHOPAEDICS, INC. · Class III
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TaperFit Cemented Hip System — CORIN LTD · Class II
Omnifit — Howmedica Osteonics Corp. · Class II
SPII Model Lubinus — WALDEMAR LINK GmbH & Co. KG · Class II
SPII Model Lubinus — WALDEMAR LINK GmbH & Co. KG · Class II

Cleared under the same submission

K955473 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Zimmer, Inc.

Sources (1)

FDA UDI a5cbb802-30ed-41d3-81b8-e82ef4498423 35 fields · synced Jun 8, 2026