InTice™ -C Porous Ti Cervical Interbody System - InTice™-C 13mm x 16mm x 9mm Parallel-Convex - Xtant Medical Holdings, Inc.

Duns Number:081224143

Device Description: InTice™-C 13mm x 16mm x 9mm Parallel-Convex

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

-

Brand Name

InTice™ -C Porous Ti Cervical Interbody System

Version/Model Number

X098-0509-STR

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K173832

Product Code Details

Product Code

ODP

Product Code Name

Intervertebral Fusion Device With Bone Graft, Cervical

Device Record Status

Public Device Record Key

bfac582d-570f-4212-8518-5ce1e3c40ebe

Public Version Date

June 03, 2021

Public Version Number

3

DI Record Publish Date

November 18, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"XTANT MEDICAL HOLDINGS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1719
2 A medical device with a moderate to high risk that requires special controls. 3162
U Unclassified 25