FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Double Internal Joint Stabilizer- Elbow

K Number: K231447 · Decision Dec 15, 2023
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
2
Applicant Total
20
Review Days
211

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Basic Information

Device Name
Double Internal Joint Stabilizer- Elbow
K Number
K231447
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Skeletal Dynamics, Inc.
Date Received
May 18, 2023
Decision Date
December 15, 2023
Product Code
OZI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OZI Internal Hinged Elbow Fixator

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Other Clearances by Skeletal Dynamics, Inc.

K Number Device Name
K254288 Clavicle Fixation System
K252949 Geminus Volar Distal Radius Plating System
K242436 Proximal Humerus Fixation System
K243381 Total Wrist Arthroplasty System (TWA)
K241815 Protean Fragment Plating System
K242055 Freefix Forearm Plating System
K240835 Suture Button Repair System
K231188 ALIGN Radial Head System
K231623 Distal Elbow Plating System
K223318 Internal Joint Stabilizer - Elbow
Search all 20 clearances from Skeletal Dynamics, Inc. →