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

ACCIN PATELLOFEMORAL SYSTEM

K Number: K073120 · Decision Feb 29, 2008
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
26
Applicant Total
7
Review Days
116

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Basic Information

Device Name
ACCIN PATELLOFEMORAL SYSTEM
K Number
K073120
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Accelerated Innovation, LLC
Date Received
November 5, 2007
Decision Date
February 29, 2008
Product Code
KRR
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
KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

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Other Clearances by Accelerated Innovation, LLC

K Number Device Name
K081127 ACCIN TOTAL KNEE SYSTEM
K080647 ACCIN BIPOLAR HEAD SYSTEM
K080539 ACCIN UNIPOLAR HEAD SYSTEM
K073531 ACCIN PEDICLE SCREW SYSTEM
K073530 ACCIN ANTERIOR CERVICAL PLATE SYSTEM
K073068 ACCIN HIP SYSTEM