ANKLE HINDFOOT NAILING SYSTEM - ANKLE HINDFOOT REVISION NAIL TI L200MM D12MM - ORTHOFIX SRL

Duns Number:438793622

Device Description: ANKLE HINDFOOT REVISION NAIL TI L200MM D12MM STERILE WITH GUIDE JIG

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More Product Details

Catalog Number

99-T772201

Brand Name

ANKLE HINDFOOT NAILING SYSTEM

Version/Model Number

1

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

K141571

Product Code Details

Product Code

HSB

Product Code Name

Rod, Fixation, Intramedullary And Accessories

Device Record Status

Public Device Record Key

74563bda-c988-4d3d-b17a-45f7a8e52966

Public Version Date

May 27, 2021

Public Version Number

1

DI Record Publish Date

May 19, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ORTHOFIX SRL" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 64
2 A medical device with a moderate to high risk that requires special controls. 6371