PONTiS Suture-Crimp Implant - PONTiS Dual Suture-Crimp Implant kit with - PONTIS ORTHOPAEDICS, LLC

Duns Number:047775061

Device Description: PONTiS Dual Suture-Crimp Implant kit with Multifilament Stainless Steel Sutures and SS Cri PONTiS Dual Suture-Crimp Implant kit with Multifilament Stainless Steel Sutures and SS CrimpEach Kit contains:1x Dual #3-0 MFSS sutures with 2 straight needles1x SS Crimp collarSupplied pouched, sterilized with EO

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More Product Details

Catalog Number

400-3020

Brand Name

PONTiS Suture-Crimp Implant

Version/Model Number

400-3020

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Unsafe

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"

Yes

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

GAQ

Product Code Name

Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile

Device Record Status

Public Device Record Key

d12cee9e-4183-43a7-ba79-aa1b29b3696d

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

September 12, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PONTIS ORTHOPAEDICS, LLC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 7