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Anatomic

FDA UDI

Class II (US FDA UDI)

by Amplitude

Identity

Trade Name
ANATOMIC FDA UDI
Generic Name
Uncoated knee femur prosthesis, metallic FDA UDI
Device Name
ANATOMIC® Posterior Stabilized Femoral Component Cemented Size 2 RIGHT FDA UDI
Model / Reference
1-0209502 FDA UDI
Description
ANATOMIC® Posterior Stabilized Femoral Component Cemented Size 2 RIGHT FDA UDI

Identifiers

Catalog Number
1-0209502 FDA UDI
Primary DI / UDI-DI
03701089500029 FDA UDI
510(k) Number
K161414 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Uncoated knee femur prosthesis, metallic 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

No

FDA UDI

Category: Uncoated knee femur prosthesis, metallic

Anatomic by Amplitude — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated knee femur prosthesis, metallic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Amplitude

Sources (1)

  • FDA UDI 31bc0645-75aa-49b1-ac7b-06c190b9409e 36 fields · synced Jun 1, 2026