ProCinch - PROCINCH NO BUTTON ADJUSTABLE LOOP IMPLANT - STRYKER CORPORATION

Duns Number:187502109

Device Description: PROCINCH NO BUTTON ADJUSTABLE LOOP IMPLANT

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More Product Details

Catalog Number

234-102-061

Brand Name

ProCinch

Version/Model Number

234-102-061

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

K210078

Product Code Details

Product Code

MBI

Product Code Name

Fastener, fixation, nondegradable, soft tissue

Device Record Status

Public Device Record Key

04e57caa-ea33-4b03-a47c-32d8a5654900

Public Version Date

June 17, 2021

Public Version Number

1

DI Record Publish Date

June 09, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STRYKER CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2188
2 A medical device with a moderate to high risk that requires special controls. 3183
U Unclassified 60