icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 090 mm - icotec Pedicle System 6.0, Rod, Ti, Curved, Ø - icotec AG

Duns Number:480789465

Device Description: icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 090 mm

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More Product Details

Catalog Number

16-60-91209

Brand Name

icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 090 mm

Version/Model Number

16-60-91209

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

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

-

Product Code Details

Product Code

NKB

Product Code Name

Thoracolumbosacral Pedicle Screw System

Device Record Status

Public Device Record Key

da78fe22-c9f8-4f86-9658-0bd01d307053

Public Version Date

August 26, 2022

Public Version Number

1

DI Record Publish Date

August 18, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ICOTEC AG" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 651