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Maestro™ Total Wrist

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Maestro™ Total Wrist FDA UDI
Generic Name
Total wrist carpal articulation prosthesis FDA UDI
Model / Reference
180063 FDA UDI

Identifiers

Catalog Number
180063 FDA UDI
Primary DI / UDI-DI
00887868239366 FDA UDI
510(k) Number
K042032 FDA UDI
FDA Product Code
JWJ FDA UDI
GMDN Term
Total wrist carpal articulation prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3800 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: Total wrist carpal articulation prosthesis

Maestro™ Total Wrist by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total wrist carpal articulation 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 1824c18a-ea54-4d35-a89a-1a7bbfda1c65 36 fields · synced Jun 8, 2026