Catalog Number

-

Brand Name

EIT ALIF Distractor Forceps

Version/Model Number

AFT10100

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

-

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

K170503

Product Code

LXH

Product Code Name

Orthopedic Manual Surgical Instrument

Public Device Record Key

441c1e30-2a3e-4772-bdb2-5248f6bce3ae

Public Version Date

August 21, 2019

Public Version Number

4

DI Record Publish Date

January 05, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-