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Rx Knee AP Symmetrical Augment Size 1 - 12mm Titanium Draft

FDA UDI

Class II (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Rx Knee AP Symmetrical Augment Size 1 - 12mm Titanium Draft FDA UDI
Generic Name
Temporary knee prosthesis, non-customized FDA UDI
Model / Reference
121-20-9261 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215111458 FDA UDI
510(k) Number
K240683 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Temporary knee prosthesis, non-customized FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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: Temporary knee prosthesis, non-customized

Rx Knee AP Symmetrical Augment Size 1 - 12mm Titanium Draft by Signature Orthopaedics Pty Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Temporary knee prosthesis, non-customized.

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 625f69fc-5c15-4924-a08b-2662e15543fd 33 fields · synced May 30, 2026