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B-P Total Knee System

FDA UDI

Class II (US FDA UDI)

by Endotec, Inc.

Identity

Trade Name
B-P TOTAL KNEE SYSTEM FDA UDI
Generic Name
Cruciate-retaining total knee prosthesis FDA UDI
Device Name
B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 3, SIZE 6 FDA UDI
Model / Reference
04-32-0026 FDA UDI
Description
B-P KNEE TIBIA PLATFORM COMPONENT, W/BIOCOAT, W/ULTRACOAT, TYPE 3, SIZE 6 FDA UDI

Identifiers

Catalog Number
04-32-0026 FDA UDI
Primary DI / UDI-DI
00814193020772 FDA UDI
510(k) Number
K012702 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Cruciate-retaining total knee prosthesis 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: Cruciate-retaining total knee prosthesis

B-P Total Knee System by Endotec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cruciate-retaining total knee prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endotec, Inc.

Sources (1)

  • FDA UDI 77c0fc35-7112-4eac-81d7-d5f0bb23032b 37 fields · synced Jun 1, 2026