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

EXPRT™ Revision Hip System - EXPRT™ Hip Distal Stem, EXPRT™ Hip Standard Offset Proximal Body Implant, EXPRT™ Hip Lateral Offset Proximal Body Implant, EXPRT™ Hip Capture Bolt

K Number: K163497 · Decision Mar 2, 2017
Classifications
1
FEI Numbers
156
Registration Numbers
156
Same Product Code
33
Applicant Total
81
Review Days
79

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Basic Information

Device Name
EXPRT™ Revision Hip System - EXPRT™ Hip Distal Stem, EXPRT™ Hip Standard Offset Proximal Body Implant, EXPRT™ Hip Lateral Offset Proximal Body Implant, EXPRT™ Hip Capture Bolt
K Number
K163497
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3310
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Medical L.P.
Date Received
December 13, 2016
Decision Date
March 2, 2017
Product Code
KWZ
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
KWZ Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

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Other Clearances by Encore Medical L.P.

K Number Device Name
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K251776 EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)
K251241 EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)
K251184 AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System
K241483 ceramys™ femoral head system
K233481 AltiVate Reverse® Glenoid
K222592 AltiVate® Anatomic Shoulder AG e+™ with Markers
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