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

BONE FRAGMENT AND FIXATION PLATES, SCREWS AND WASHERS

K Number: K130614 · Decision Jan 17, 2014
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
2
Review Days
316

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Basic Information

Device Name
BONE FRAGMENT AND FIXATION PLATES, SCREWS AND WASHERS
K Number
K130614
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Laura Cattabriga
Date Received
March 7, 2013
Decision Date
January 17, 2014
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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Other Clearances by Laura Cattabriga

K Number Device Name
K130613 CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM