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AOS CLAVICLE INTRAMEDULLARY DEVICE 3.5mm x 80mm

FDA UDI

Class II (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
AOS CLAVICLE INTRAMEDULLARY DEVICE 3.5mm x 80mm FDA UDI
Generic Name
Clavicle intramedullary nail-like rod FDA UDI
Model / Reference
1300-080 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665021202 FDA UDI
510(k) Number
K143204 FDA UDI
FDA Product Code
JDW FDA UDI
HSB FDA UDI
GMDN Term
Clavicle intramedullary nail-like rod FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3020 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Clavicle intramedullary nail-like rod

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Similar devices

Also classified as Clavicle intramedullary nail-like rod.

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 1286d89d-d8d2-42cd-afc1-3596d26d53b2 33 fields · synced Jun 20, 2026