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

RESTORATION ACETABULAR WEDGE AUGMENTS

K Number: K102019 · Decision Mar 3, 2011
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
13
Review Days
227

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Basic Information

Device Name
RESTORATION ACETABULAR WEDGE AUGMENTS
K Number
K102019
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics
Date Received
July 19, 2010
Decision Date
March 3, 2011
Product Code
LPH
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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

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Other Clearances by Howmedica Osteonics

K Number Device Name
K120578 ACCOLADE II HIP STEM
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K032855 STRYKER SPINE MAPS SYSTEM
K031702 REFLEX ANTERIOR CERVICAL PLATE SYSTEM
K031435 BONESOURCE BVF
K031217 GMRS PRESS FIT STEMS WITH PUREFIX HA
K022461 S2 FEMORAL NAIL
K022160 XIA SPINAL SYSTEM
K013772 MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM
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