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

2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM

K Number: K101536 · Decision Sep 15, 2010
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
5
Review Days
104

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Basic Information

Device Name
2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM
K Number
K101536
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes (Usa), LLC
Date Received
June 3, 2010
Decision Date
September 15, 2010
Product Code
HRS
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
HRS Plate, Fixation, Bone

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K Number Device Name
K180821 TruMatch Graft Cage - Long Bone
K152239 Zero-P Natural Plate System
K130146 SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM
K120275 SYNTHES ACIS/VERTEBRAL SPACER CR