Persona® PPS® 42-5080-070-01

by Zimmer, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00889024631199 UDI-DI	Date23 Nov 2022Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Persona® PPS®
Generic Name: Coated knee femur prosthesis
Model / Ref / Catalog: 42-5080-070-01

Primary DI / UDI-DI: 00889024631199
510(k) Number: K221479
FDA Product Code: OIY, MBH, JWH
GMDN Term: Coated knee femur prosthesis

Device Class: Class II
Regulation Number: 888.3560, 888.3565
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Conditional

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Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (8)

Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No