Medical Device Manufacturer · US , Washington, Dc , DC

Stanmore Implants Worldwide , Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2011
8
Total
8
Cleared
0
Denied

Stanmore Implants Worldwide , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.

Historical record: 8 cleared submissions from 2011 to 2015. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Stanmore Implants Worldwide , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Stanmore Implants Worldwide , Ltd.
8 devices
1-8 of 8
Cleared Jan 20, 2015
PATIENT SPECIFIC DISTAL FEMORAL
K140898 · KRO
Orthopedic · 287d
Cleared Jan 22, 2014
JTS EXTENDIBLE DISTAL FEMORAL IMPLANT
K133152 · KRO
Orthopedic · 61d
Cleared Jan 11, 2013
SCULPTOR ROBOTIC GUIDANCE ARM (RGA)
K121765 · OLO
Orthopedic · 210d
Cleared Sep 20, 2012
METS MODULAR PROXIMAL FEMUR
K121056 · JDI
Orthopedic · 167d
Cleared Sep 19, 2012
METS MODULAR DISTAL FEMUR
K121029 · KRO
Orthopedic · 167d
Cleared Sep 19, 2012
METS MODULAR TOTAL FEMUR
K121055 · JDI
Orthopedic · 166d
Cleared Sep 05, 2012
METS SMILES TOTAL KNEE REPLACEMENT
K120992 · KRO
Orthopedic · 156d
Cleared Mar 22, 2011
JTS EXTENDEABLE IMPLANT
K092138 · KRO
Orthopedic · 615d
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