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CxHA™

FDA UDI

Class II (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name
CxHA™ FDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
SST FDA UDI
Model / Reference
LS-457-07 FDA UDI
Description
SST FDA UDI

Identifiers

Catalog Number
LS-457-07 FDA UDI
Primary DI / UDI-DI
M711LS457070 FDA UDI
510(k) Number
K181115 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

Dimensions & Sizes

Size
Length — 16 Millimeter FDA UDI
Width — 18 Millimeter FDA UDI
Height — 12 Millimeter FDA UDI
Angle — 8 degree FDA UDI

Category: Spinal implant trial

CxHA™ by Innovasis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal implant trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovasis, Inc.

Sources (1)

  • FDA UDI 683bb58d-7389-414d-b7c6-2c7eba7d4688 37 fields · synced Jun 1, 2026