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MUTARS® femoral stem cementless

FDA UDI

Class II (US FDA UDI)

by implantcast GmbH

Identity

Trade Name
MUTARS® femoral stem cementless FDA UDI
Generic Name
Press-fit hip femur prosthesis, modular FDA UDI
Model / Reference
57600512 FDA UDI

Identifiers

Primary DI / UDI-DI
04048844049782 FDA UDI
510(k) Number
K181778 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Press-fit hip femur 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

No

FDA UDI

Category: Press-fit hip femur prosthesis, modular

MUTARS® femoral stem cementless by implantcast GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit hip femur prosthesis, modular.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
implantcast GmbH

Sources (1)

  • FDA UDI 1d340a47-c95b-4264-bcea-0116820344df 34 fields · synced Jun 8, 2026