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P.f.c.

FDA UDI

Class II (US FDA UDI)

by Depuy International Ltd

Identity

Trade Name
P.F.C. FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
P.F.C. Total Hip System FEMORAL HEAD Diameter 28mm +0 10/12 TAPER FDA UDI
Model / Reference
85-3831 FDA UDI
Description
P.F.C. Total Hip System FEMORAL HEAD Diameter 28mm +0 10/12 TAPER FDA UDI

Identifiers

Catalog Number
853831 FDA UDI
Primary DI / UDI-DI
10603295207597 FDA UDI
510(k) Number
K893872 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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: Metallic femoral head prosthesis

P.f.c. by Depuy International Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

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 89dab429-26d6-409f-80f0-e88f05a55dc0 36 fields · synced May 30, 2026