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

OPTERTRAK LOGIC PSC TIBIAL INSERT

K Number: K110547 · Decision Apr 14, 2011
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
2
Review Days
48

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Basic Information

Device Name
OPTERTRAK LOGIC PSC TIBIAL INSERT
K Number
K110547
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exactech Sarasota
Date Received
February 25, 2011
Decision Date
April 14, 2011
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWH), ordered by most recent decision date.

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Other Clearances by Exactech Sarasota

K Number Device Name
K140645 GIBRALT ROD-TO-ROD CROSS CONNECTORS