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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
5026-8-120 FDA UDI
Description
Self-drilling Half Pin FDA UDI

Identifiers

Catalog Number
5026-8-120 FDA UDI
Primary DI / UDI-DI
07613252442783 FDA UDI
510(k) Number
K121252 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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 — 5.0 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

K121252 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 2a80462f-e363-4128-98a1-79464d62c1bc 36 fields · synced May 31, 2026