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

METS SMILES TOTAL KNEE REPLACEMENT

K Number: K120992 · Decision Sep 5, 2012
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
85
Applicant Total
8
Review Days
156

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Basic Information

Device Name
METS SMILES TOTAL KNEE REPLACEMENT
K Number
K120992
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3510
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stanmore Implants Worldwide , Ltd.
Date Received
April 2, 2012
Decision Date
September 5, 2012
Product Code
KRO
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
KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

Similar 510(k) Clearances

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

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Other Clearances by Stanmore Implants Worldwide , Ltd.

K Number Device Name
K140898 PATIENT SPECIFIC DISTAL FEMORAL
K133152 JTS EXTENDIBLE DISTAL FEMORAL IMPLANT
K121765 SCULPTOR ROBOTIC GUIDANCE ARM (RGA)
K121056 METS MODULAR PROXIMAL FEMUR
K121029 METS MODULAR DISTAL FEMUR
K121055 METS MODULAR TOTAL FEMUR
K092138 JTS EXTENDEABLE IMPLANT