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

ENCORE SHOULDER REVISION GLENOID

K Number: K081448 · Decision Sep 30, 2008
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
36
Applicant Total
81
Review Days
130

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Basic Information

Device Name
ENCORE SHOULDER REVISION GLENOID
K Number
K081448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3670
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Medical L.P.
Date Received
May 23, 2008
Decision Date
September 30, 2008
Product Code
MBF
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
MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

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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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