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Ortho Solutions Succession Afn System

FDA UDI

Class II (US FDA UDI)

by Ortho Solutions Holdings Limited

Identity

Trade Name
ORTHO SOLUTIONS SUCCESSION AFN SYSTEM FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
SUCCESSION NAIL ASSEMBLY 10MM X 220MM FDA UDI
Model / Reference
OS351022-S FDA UDI
Description
SUCCESSION NAIL ASSEMBLY 10MM X 220MM FDA UDI

Identifiers

Catalog Number
OS351022-S FDA UDI
Primary DI / UDI-DI
05055662970692 FDA UDI
510(k) Number
K250622 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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: Arthrodesis intramedullary nail, non-distracting

Ortho Solutions Succession Afn System by Ortho Solutions Holdings Limited — 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 afa102d7-7989-49a3-85e3-181bb038b4a5 36 fields · synced May 30, 2026