PolyLock Ankle Plates - Lateral Fibula Plate Universal Revision 11 Hole - FUSION ORTHOPEDICS, LLC

Duns Number:080307067

Device Description: Lateral Fibula Plate Universal Revision 11 Hole

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More Product Details

Catalog Number

AK-LF-2911

Brand Name

PolyLock Ankle Plates

Version/Model Number

AK-LF-2911

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

K202959

Product Code Details

Product Code

HRS

Product Code Name

Plate, Fixation, Bone

Device Record Status

Public Device Record Key

bd8ec1b7-380b-44ae-bdae-49a7e1e9ee87

Public Version Date

January 31, 2022

Public Version Number

1

DI Record Publish Date

January 21, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FUSION ORTHOPEDICS, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 10
2 A medical device with a moderate to high risk that requires special controls. 1516