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King Cobra

FDA UDI

Class II (US FDA UDI)

by Eminent Spine Llc

Identity

Trade Name
King Cobra FDA UDI
Generic Name
External spinal fixation system FDA UDI
Model / Reference
KCP644 FDA UDI

Identifiers

Primary DI / UDI-DI
B014KCP644 FDA UDI
510(k) Number
K103068 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
External spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: External spinal fixation system

King Cobra by Eminent Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External spinal fixation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eminent Spine Llc

Sources (1)

  • FDA UDI c8a3dd60-0262-4e54-b5e6-a0f0e0687cce 33 fields · synced May 30, 2026