InterSpace Tapered Wedge Stem Trial - InterSpace Tapered Wedge Stem Trial is intended - TECRES SPA

Duns Number:435428396

Device Description: InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of the right InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem to be implanted.

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More Product Details

Catalog Number

-

Brand Name

InterSpace Tapered Wedge Stem Trial

Version/Model Number

SPC90Z3

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

-

Product Code Details

Product Code

HWT

Product Code Name

Template

Device Record Status

Public Device Record Key

d1bbac04-29e5-4e72-be0b-6371dfa9ab55

Public Version Date

October 03, 2022

Public Version Number

1

DI Record Publish Date

September 23, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"TECRES SPA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 37
2 A medical device with a moderate to high risk that requires special controls. 52