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Apex

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
APEX FDA UDI
Generic Name
Orthopaedic bone pin, non-bioabsorbable FDA UDI
Device Name
Self-drilling Half Pin FDA UDI
Model / Reference
5018-5-200 FDA UDI
Description
Self-drilling Half Pin FDA UDI

Identifiers

Catalog Number
5018-5-200 FDA UDI
Primary DI / UDI-DI
07613327091960 FDA UDI
510(k) Number
K861766 FDA UDI
FDA Product Code
JDW FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 200.0 Millimeter FDA UDI

Category: Orthopaedic bone pin, non-bioabsorbable

Apex by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 1b695a93-c0b7-4aef-86ec-698d505eb070 36 fields · synced Jun 8, 2026