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Salvation™

FDA UDI

Class I (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
SALVATION™ FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
K-WIRE FDA UDI
Model / Reference
SMN10017 FDA UDI
Description
K-WIRE FDA UDI

Identifiers

Catalog Number
SMN10017 FDA UDI
Primary DI / UDI-DI
00889797076845 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic bone wire

Salvation™ by Wright Medical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone wire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12f7f10e-38ad-4941-8cad-f3b8e0b5eede 36 fields · synced Jun 8, 2026