Titan™ - The Titan Modular Total Shoulder system is - Ascension Orthopedics, Inc.

Duns Number:942377524

Device Description: The Titan Modular Total Shoulder system is indicated for painful and/or disabled joints, f The Titan Modular Total Shoulder system is indicated for painful and/or disabled joints, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable. The Humeral 2.5 set includes centric and eccentric humeral head trials to evaluate the size and fit of the appropriate implants. Head sizing plates are included to find the base width, as well as determine the need for concentric or eccentric, prior to trialing the humeral head. Instruments to assist with the trials and sizing are also included in the set.

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More Product Details

Catalog Number

-

Brand Name

Titan™

Version/Model Number

TITANH2IMP

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

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

K142413

Product Code Details

Product Code

HSD

Product Code Name

PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

Device Record Status

Public Device Record Key

3d392f65-236f-450c-bc81-282fee0be9ef

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 15, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ASCENSION ORTHOPEDICS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1909
2 A medical device with a moderate to high risk that requires special controls. 1404
3 A medical device with high risk that requires premarket approval 12
U Unclassified 15