← Back to catalogue

Inertia® CONNEXX™ Modular Pedicle Screw System

FDA UDI

Class II (US FDA UDI)

by Nexxt Spine Llc

Identity

Trade Name
Inertia® CONNEXX™ Modular Pedicle Screw System FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Open Screw Instrument Tray FDA UDI
Model / Reference
C20-01-01 FDA UDI
Description
Open Screw Instrument Tray FDA UDI

Identifiers

Primary DI / UDI-DI
00889929050422 FDA UDI
510(k) Number
K221905 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Inertia® CONNEXX™ Modular Pedicle Screw System by Nexxt Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Cleared under the same submission

K221905 also covers:

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
Nexxt Spine Llc

Sources (1)

  • FDA UDI 45642043-07e1-4f96-9a46-b318f263f2a9 35 fields · synced Jun 8, 2026