Dorsal Nail Plate, Anatomical

FDA 510(k) K052248 · Hand Innovations, LLC

Substantially Equivalent

510(k) numberK052248

Submission

Device name
Dorsal Nail Plate, Anatomical
Applicant
Hand Innovations, LLC
Miami Lakes, FL, US
Received
August 18, 2005
Decision date
September 14, 2005
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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K261511Xpert AnkleHRS · Traditional Newclip Technics07/28/2026SE
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K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion…HRS · Special TriMed, Inc.07/16/2026SE
K261191Alians Elbow SHRS · Traditional Newclip Technics07/08/2026SE
K261054RibPlate SystemHRS · Traditional Stryker Leibinger GmbH & Co KG07/01/2026SE
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More from Bonebridge AG

510(k)DeviceDecision
K061748Fragment Plate SystemKTT · Special 07/17/2006SE
K060864Multidirectional Threaded PegLXT · Special 04/28/2006SE
K060294Diaphyseal PlateHRS · Traditional 03/22/2006SE
K060290Shoulder Fixation SystemLXT · Special 02/27/2006SE
K052294Shoulder Nail PlateHRS · Traditional 10/21/2005SE
K051728Modification to Shoulder Fixation SystemLXT · Special 07/20/2005SE
K050932Distal Volar Radius Anatomical Plate SystemLXT · Special 04/26/2005SE
K042059Shoulder Fixation SystemLXT · Traditional 09/30/2004SE
K041157Modification to Small Bone Fixation SystemHTY · Traditional 07/30/2004SE
K041081Fragment Plate System, Screws, Pins and K-WiresKTT · Traditional 07/01/2004SE

Questions and answers

When was Dorsal Nail Plate, Anatomical cleared by the FDA?

Dorsal Nail Plate, Anatomical (K052248) received a 510(k) decision of Substantially Equivalent on September 14, 2005, 27 days after the submission was received.

What is the product code of K052248?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.