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

Suture Button Repair System

K Number: K240835 · Decision Jul 19, 2024
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
20
Review Days
115

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Suture Button Repair System
K Number
K240835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Skeletal Dynamics, Inc.
Date Received
March 26, 2024
Decision Date
July 19, 2024
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MBI), ordered by most recent decision date.

View all

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
K231447 Double Internal Joint Stabilizer- Elbow
K231188 ALIGN Radial Head System
K231623 Distal Elbow Plating System
K223318 Internal Joint Stabilizer - Elbow
Search all 20 clearances from Skeletal Dynamics, Inc. →