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APEX Spine System

FDA UDI

Class II (US FDA UDI)

by Spinecraft Llc

Identity

Trade Name
APEX Spine System FDA UDI
Generic Name
Bone-screw internal spinal fixation system rod FDA UDI
Device Name
Titanium Rod 6.0 x 40mm, Straight FDA UDI
Model / Reference
6000-040 FDA UDI
Description
Titanium Rod 6.0 x 40mm, Straight FDA UDI

Identifiers

Primary DI / UDI-DI
M82460000401 FDA UDI
510(k) Number
K062513 FDA UDI
K092825 FDA UDI
K102488 FDA UDI
K110906 FDA UDI
K132603 FDA UDI
FDA Product Code
NKB FDA UDI
MNI FDA UDI
MNH FDA UDI
KWQ FDA UDI
KWP FDA UDI
GMDN Term
Bone-screw internal spinal fixation system rod FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3060 FDA UDI
888.3050 FDA UDI
Commercial Distribution
Not 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

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

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

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Manufacturer

Manufacturer
Spinecraft Llc

Sources (1)

  • FDA UDI 4fc0f0a9-de3b-410d-9925-7a84fadd24df 36 fields · synced May 31, 2026