Equinoxe - Exactech, Inc.

Duns Number:157565946

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More Product Details

Catalog Number

SPI-037397

Brand Name

Equinoxe

Version/Model Number

SPI-037397

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

K063569,K193098,K150458,K131575,K110708,K102951,K101909,K093275,K082702,K073688

Product Code Details

Product Code

KWS

Product Code Name

Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Device Record Status

Public Device Record Key

556b40cd-3be3-4320-97d5-1fc31d8f601b

Public Version Date

October 19, 2021

Public Version Number

1

DI Record Publish Date

October 11, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"EXACTECH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3717
2 A medical device with a moderate to high risk that requires special controls. 7206
3 A medical device with high risk that requires premarket approval 28