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Ø3.5mm x 20mm Precontoured Cervical Rods

FDA UDI

Class II (US FDA UDI)

by Xenco Medical Llc

Identity

Trade Name
Ø3.5mm x 20mm Precontoured Cervical Rods FDA UDI
Generic Name
Bone-screw internal spinal fixation system rod FDA UDI
Model / Reference
XM-217-0020 FDA UDI

Identifiers

Primary DI / UDI-DI
B064XM21700201 FDA UDI
FDA Product Code
KWP FDA UDI
NKG FDA UDI
GMDN Term
Bone-screw internal spinal fixation system rod FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system rod

Ø3.5mm x 20mm Precontoured Cervical Rods by Xenco Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system rod.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xenco Medical Llc

Sources (1)

  • FDA UDI 7f86273e-2b63-4c62-8006-74b82a2fec1e 33 fields · synced Jun 1, 2026