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

Biomet Variable Pitch Compression Screw System

K Number: K160058 · Decision Mar 9, 2016
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
441
Review Days
57

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Basic Information

Device Name
Biomet Variable Pitch Compression Screw System
K Number
K160058
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet, Inc.
Date Received
January 12, 2016
Decision Date
March 9, 2016
Product Code
HWC
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
HWC Screw, Fixation, Bone

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K213287 StageOne Knee Cement Spacer Molds
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K210192 A.L.P.S. Clavicle Plating System
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K193546 Distal Centralizers
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