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Trabecular Metal Reverse Plus™

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Trabecular Metal Reverse Plus™ FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Model / Reference
00430508010 FDA UDI

Identifiers

Catalog Number
00-4305-080-10 FDA UDI
Primary DI / UDI-DI
00889024489608 FDA UDI
510(k) Number
K172767 FDA UDI
FDA Product Code
PHX FDA UDI
KWT FDA UDI
KWS FDA UDI
HSD FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3650 FDA UDI
888.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Trabecular Metal Reverse Plus™ by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 31ee0864-37d4-4f7a-b686-eeb9ce625517 35 fields · synced May 30, 2026