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

SurgTech Bipolar Head System

K Number: K173455 · Decision Jun 14, 2018
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
98
Applicant Total
6
Review Days
219

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Basic Information

Device Name
SurgTech Bipolar Head System
K Number
K173455
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3390
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surgtech, Inc.
Date Received
November 7, 2017
Decision Date
June 14, 2018
Product Code
KWY
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
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

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K162125 MALUC™ Total Hip Arthroplasty System
K163363 SurgTech Thoracolumbosacral (TLS) Posterior Fixation System
K161894 SurgTech Trauma System
K152200 SurgTech Interbody System