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Cancellous locking screw, Ø6.5 × 20mm

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
Cancellous locking screw, Ø6.5 × 20mm FDA UDI
Generic Name
Acetabular shell FDA UDI
Device Name
Cancellous locking screw, Ø6.5 × 20mm FDA UDI
Model / Reference
5208-1020 FDA UDI
Description
Cancellous locking screw, Ø6.5 × 20mm FDA UDI

Identifiers

Catalog Number
5208-1020 FDA UDI
Primary DI / UDI-DI
04719872154563 FDA UDI
510(k) Number
K163441 FDA UDI
FDA Product Code
LZO FDA UDI
JDI FDA UDI
GMDN Term
Acetabular shell FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3350 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: Acetabular shell

Cancellous locking screw, Ø6.5 × 20mm by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular shell.

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 3527cfd6-7127-4f40-a368-f1dc1a05e7a3 37 fields · synced May 30, 2026