Catalog Number

50116-S

Brand Name

Jigsaw Medical, LLC

Version/Model Number

50116-S

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

NBH

Product Code Name

Accessories, Arthroscopic

Public Device Record Key

ffc65774-1858-431d-a15e-555f8e80a411

Public Version Date

February 06, 2020

Public Version Number

2

DI Record Publish Date

September 19, 2019

Package DI Number

00856274008248

Quantity per Package

6

Contains DI Package

00856274008064

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case