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

OsteoCentric Integrated Hip Fastener System

K Number: K210247 · Decision Apr 30, 2021
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
22
Applicant Total
1
Review Days
91

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Basic Information

Device Name
OsteoCentric Integrated Hip Fastener System
K Number
K210247
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteocentric Technologies D.B.A. Osteocentric Trauma
Date Received
January 29, 2021
Decision Date
April 30, 2021
Product Code
JDO
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
JDO Device, Fixation, Proximal Femoral, Implant

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