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Control

FDA UDI

Class II (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
CONTROL FDA UDI
Generic Name
Orthopaedic bone cerclage wire FDA UDI
Device Name
CONTROL CABLE CABLE & SLEEVE - COBALT CHROME 1.8mm x 24 Inches FDA UDI
Model / Reference
1739-28-000 FDA UDI
Description
CONTROL CABLE CABLE & SLEEVE - COBALT CHROME 1.8mm x 24 Inches FDA UDI

Identifiers

Catalog Number
173928000 FDA UDI
Primary DI / UDI-DI
10603295067788 FDA UDI
510(k) Number
K934557 FDA UDI
FDA Product Code
JDQ FDA UDI
GMDN Term
Orthopaedic bone cerclage wire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3010 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: Orthopaedic bone cerclage wire

Control by Depuy Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone cerclage wire.

Cleared under the same submission

K934557 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Orthopaedics, Inc.

Sources (1)

  • FDA UDI 293335a0-8491-40a8-977b-f2006773e9fa 36 fields · synced Jun 8, 2026