SMR Shoulder - Glenoid Drill Peg S - LIMACORPORATE SPA

Duns Number:432066322

Device Description: Glenoid Drill Peg S

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More Product Details

Catalog Number

9CCS.13.002

Brand Name

SMR Shoulder

Version/Model Number

9CCS.13.002

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

K163397

Product Code Details

Product Code

KWS

Product Code Name

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

Device Record Status

Public Device Record Key

72d51b05-c3f8-427d-bfd1-ea9fb8e4724f

Public Version Date

February 14, 2022

Public Version Number

1

DI Record Publish Date

February 05, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"LIMACORPORATE SPA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 595
2 A medical device with a moderate to high risk that requires special controls. 3634