← Back to catalogue

Adapter for BIOLOX OPTION Femoral Head, +7mm head length

FDA UDI

Class II (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name
Adapter for BIOLOX OPTION Femoral Head, +7mm head length FDA UDI
Generic Name
Ceramic femoral head prosthesis FDA UDI
Model / Reference
3301.00.700 FDA UDI

Identifiers

Primary DI / UDI-DI
00814703011658 FDA UDI
510(k) Number
K143407 FDA UDI
FDA Product Code
LPH FDA UDI
MBL FDA UDI
LZO FDA UDI
GMDN Term
Ceramic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Ceramic femoral head prosthesis

Adapter for BIOLOX OPTION Femoral Head, +7mm head length by Total Joint Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Ceramic femoral head prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 04eaef31-adba-464b-8fc2-f437f0b735d4 36 fields · synced Jun 6, 2026