DEVICE: KATOR, LLC (B18610305920)

Device Identifier (DI) Information

KATOR, LLC
1030592
In Commercial Distribution
1030592
KATOR, LLC
B18610305920
HIBCC

1
080346102 *Terms of Use
KATOR Suture Anchor, Arthroscopic, 5.0mm x 25mm, #2 Suture
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name GMDN Definition
Ligament anchor A device designed to be implanted into bone specifically to attach the ends of a ligament (synthetic or natural source) to the bone. The device is available in various designs and sizes and is made of a material that cannot be chemically degraded or absorbed via natural body processes [e.g., titanium (Ti)].
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FDA Product Code

[?]
Product Code Product Code Name
MBI Fastener, Fixation, Nondegradable, Soft Tissue
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K152236 000
No CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

62a9feee-a553-4c5f-81d3-cdc546a595ff
July 06, 2018
3
August 17, 2016
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

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Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
No Customer Contact currently defined
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