IMPLANET SPINE SYSTEM - IMPLANET

Duns Number:291993439

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More Product Details

Catalog Number

550306

Brand Name

IMPLANET SPINE SYSTEM

Version/Model Number

Ø4.0 Snap-on Tap

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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)

-

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

af0c5f54-1985-4fab-aef4-d8b7103f5e9d

Public Version Date

September 28, 2018

Public Version Number

1

DI Record Publish Date

August 28, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"IMPLANET" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 236
2 A medical device with a moderate to high risk that requires special controls. 828