Catalog Number

-

Brand Name

VSP Orthopedics

Version/Model Number

Patient Tibia Template

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

-

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

K190044

Product Code

PBF

Product Code Name

Orthopaedic Surgical Planning And Instrument Guides

Public Device Record Key

6c4e791f-1a3f-4941-ad4d-543ac678a793

Public Version Date

December 04, 2020

Public Version Number

2

DI Record Publish Date

September 11, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-