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Origin DAA Stem, Coxa Vara

FDA UDI

Class II (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Origin DAA Stem, Coxa Vara FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Model / Reference
111-39-1604 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215092818 FDA UDI
510(k) Number
K161155 FDA UDI
FDA Product Code
MEH FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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

Yes

FDA UDI

Category: Coated femoral stem prosthesis, modular

Origin DAA Stem, Coxa Vara by Signature Orthopaedics Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

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 12ab5264-5561-4dc3-944d-6d32b2905cc1 33 fields · synced May 30, 2026