PERPOS PLS Removal Driver Kit - 1 Removal Driver, 2 Pin Drivers - INTERVENTIONAL SPINE, INC

Duns Number:017663522

Device Description: 1 Removal Driver, 2 Pin Drivers

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More Product Details

Catalog Number

9068-00

Brand Name

PERPOS PLS Removal Driver Kit

Version/Model Number

9068-00

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 23, 2016

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

-

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

LXH

Product Code Name

Orthopedic Manual Surgical Instrument

Device Record Status

Public Device Record Key

8f28d8b8-bed8-4c9d-8285-61e5ee595d8b

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 15, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INTERVENTIONAL SPINE, INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 150
2 A medical device with a moderate to high risk that requires special controls. 132
U Unclassified 13