APEX Spine System

FDA UDI

Class II (US FDA UDI)

by Spinecraft Llc

Identity

Trade Name: APEX Spine System FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: APEX Ti Poly Reduction Screw, Dia.6.25, 60mm, Self-Tapping FDA UDI
Model / Reference: PR6-6260-F FDA UDI
Description: APEX Ti Poly Reduction Screw, Dia.6.25, 60mm, Self-Tapping FDA UDI

Identifiers

Catalog Number: PR6-6260-F FDA UDI
Primary DI / UDI-DI: 00193082016936 FDA UDI
510(k) Number: K062513 FDA UDI
K092825 FDA UDI
K102488 FDA UDI
K110906 FDA UDI
K132603 FDA UDI
FDA Product Code: MNH FDA UDI
KWP FDA UDI
NKB FDA UDI
MNI FDA UDI
KWQ FDA UDI
GMDN Term: Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3050 FDA UDI
888.3060 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable

APEX Spine System by Spinecraft Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

4CIS® Chiron Spinal Fixation System — ALPHANOX CO., LTD. · Class II
LnK/PathLoc-L MIS Spinal System — L&K BIOMED CO. , LTD. · Class II
ASPIRON™ ACPSYSTEM — CG MedTech Co., Ltd. · Class II
Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
OpenLoc-L Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · Class II

Cleared under the same submission

K062513 also covers:

K092825 also covers:

K102488 also covers:

K110906 also covers:

K132603 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Spinecraft Llc

Sources (1)

FDA UDI e0b4589e-f4bb-492f-80f9-7f8c0dede05d 36 fields · synced May 30, 2026