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

WishBone K-Wire System

K Number: K173013 · Decision Dec 14, 2017
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
8
Review Days
78

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
WishBone K-Wire System
K Number
K173013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Wishbone Medical, Inc.
Date Received
September 27, 2017
Decision Date
December 14, 2017
Product Code
HTY
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
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

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

View all

Other Clearances by Wishbone Medical, Inc.

K Number Device Name
K231461 Smart Correction System (HA Half Pins)
K230527 WishBone Medical Plate and Screw System
K221366 Smart Correction System Rings and Compatible HA-Coated Half Pins
K213489 Wishbone Medical Plate and Screw System: 3.0mm Screws and 7-Hole Straight Fibula Plate
K203467 WishBone Medical Plate and Screw System
K193368 Smart Correction System
K180736 WishBone Medical Plate and Screw System