← Back to catalogue

Tyber Medical

FDA UDI

Class II (US FDA UDI)

by Tyber Medical

Identity

Trade Name
Tyber Medical FDA UDI
Generic Name
Intervertebral-body internal spinal fixation system FDA UDI
Model / Reference
ACP Level 2, 42 mm FDA UDI

Identifiers

Catalog Number
20405422S FDA UDI
Primary DI / UDI-DI
M69520405422S1 FDA UDI
510(k) Number
K103068 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Intervertebral-body internal 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intervertebral-body internal spinal fixation system

Tyber Medical by Tyber Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intervertebral-body internal spinal fixation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tyber Medical

Sources (1)

  • FDA UDI 14b67142-398e-496c-8ed6-9d506aef8058 34 fields · synced Jun 1, 2026