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MUTARS® proximal femur incl. safety screw

FDA UDI

Class II (US FDA UDI)

by implantcast GmbH

Identity

Trade Name
MUTARS® proximal femur incl. safety screw FDA UDI
Generic Name
Uncoated hip femur prosthesis, modular FDA UDI
Model / Reference
57100207 FDA UDI

Identifiers

Primary DI / UDI-DI
04048844045760 FDA UDI
510(k) Number
K181778 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Uncoated 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

Yes

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 hip femur prosthesis, modular

MUTARS® proximal femur incl. safety screw by implantcast GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated 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 d0262f96-483e-46ea-bfa1-9268fe6b9dd4 34 fields · synced May 31, 2026