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P.f.c.

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
P.F.C. FDA UDI
Generic Name
Uncoated knee tibia prosthesis, polyethylene FDA UDI
Device Name
P.F.C. TIBIAL TRAY FIXED BEARING MODULAR PLUS 3 CEMENTED FDA UDI
Model / Reference
86-0123 FDA UDI
Description
P.F.C. TIBIAL TRAY FIXED BEARING MODULAR PLUS 3 CEMENTED FDA UDI

Identifiers

Catalog Number
860123 FDA UDI
Primary DI / UDI-DI
10603295215448 FDA UDI
510(k) Number
K241000 FDA UDI
K884796 FDA UDI
K923807 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Uncoated knee tibia prosthesis, polyethylene 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

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
MRI Safety
MR Conditional FDA UDI

Category: Uncoated knee tibia prosthesis, polyethylene

P.f.c. by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated knee tibia prosthesis, polyethylene.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI dcca5200-8bed-41fb-8b3b-49abdab8c18a 36 fields · synced May 31, 2026