← Back to catalogue

AOS SOLID LOCKING LAG SCREW 10.5mm x 105mm

FDA UDI

Class II (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
AOS SOLID LOCKING LAG SCREW 10.5mm x 105mm FDA UDI
Generic Name
Femur intramedullary nail FDA UDI
Model / Reference
S1094-105 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665011173 FDA UDI
510(k) Number
K120148 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Femur intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
Not 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

AOS SOLID LOCKING LAG SCREW 10.5mm x 105mm by Advanced Orthopaedic Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c803dc9d-6ac2-4ba4-843f-e55c0cdc412d 34 fields · synced May 30, 2026