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Orthopedic Salvage System (OSS™)

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Orthopedic Salvage System (OSS™) FDA UDI
Generic Name
Uncoated knee femur prosthesis, metallic FDA UDI
Model / Reference
CP114849 FDA UDI

Identifiers

Catalog Number
CP114849 FDA UDI
Primary DI / UDI-DI
00880304703421 FDA UDI
510(k) Number
K140509 FDA UDI
FDA Product Code
KRO FDA UDI
JDI FDA UDI
KRQ FDA UDI
GMDN Term
Uncoated knee femur prosthesis, metallic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3510 FDA UDI
888.3350 FDA UDI
888.3550 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

Orthopedic Salvage System (OSS™) by Biomet Orthopedics, Inc. — 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

Sources (1)

  • FDA UDI 8ee77915-6cfb-4141-b726-72a5b8a91a42 36 fields · synced May 30, 2026