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Salvation

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
SALVATION FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
Midfoot Nail FDA UDI
Model / Reference
SMN08110 FDA UDI
Description
Midfoot Nail FDA UDI

Identifiers

Catalog Number
SMN08110 FDA UDI
Primary DI / UDI-DI
00889797070539 FDA UDI
510(k) Number
K180024 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 110 Millimeter FDA UDI
Outer Diameter — 8 Millimeter FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

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

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

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 45613a21-552b-4f88-8d95-3cd507adb6d8 37 fields · synced Jun 8, 2026