PERLA ® TL MIS - XTAB CANNULATED FENESTRATED SAGITTAL SCREW - SpineArt SA

Duns Number:483016148

Device Description: XTAB CANNULATED FENESTRATED SAGITTAL SCREW

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More Product Details

Catalog Number

MPF-SX 85 50-S

Brand Name

PERLA ® TL MIS

Version/Model Number

MPF-SX 85 50-S

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

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

-

Product Code Details

Product Code

KWP

Product Code Name

Appliance, Fixation, Spinal Interlaminal

Device Record Status

Public Device Record Key

47f08371-23ec-40b7-b196-a7d41f452d7f

Public Version Date

February 17, 2022

Public Version Number

1

DI Record Publish Date

February 09, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SPINEART SA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 974
2 A medical device with a moderate to high risk that requires special controls. 5209