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

SPECIAL ORTHOPAEDIC SOLUTIONS GLENOID SHOULDER COMPONENT

K Number: K103104 · Decision Nov 22, 2010
Classifications
1
FEI Numbers
218
Registration Numbers
218
Same Product Code
189
Applicant Total
288
Review Days
33

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Basic Information

Device Name
SPECIAL ORTHOPAEDIC SOLUTIONS GLENOID SHOULDER COMPONENT
K Number
K103104
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics Corp.
Date Received
October 20, 2010
Decision Date
November 22, 2010
Product Code
KWS
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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

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K130895 REUNION RSA SHOULDER SYSTEM
K123604 ABG III MONOLITHIC HIP STEM
K122015 DISTAL FEMORAL GROWING PROSTHESIS, TIBIAL ROTATING COMPONENTS, BEARING, AXIS, CIRCLIP, WEDGE
K123166 TRIATHLON ALL-POLYETHYLENE CONDYLAR STABILIZING (CS) TIBIAL IMPLANTS TRIATHLON ALL-POLYETHYLENE POSTERIOR STABILIZING (P
K122853 NOVEL FIT AND FILL STEM
K121315 STRYKER CMF MEDPOR CUSTOMIZED IMPLANT
K121308 HIP SYSTEMS
K113409 S2 FEMORAL A/R NAIL S2 FEMORAL COMRESSION NAIL S2 TIBIAL NAIL S2 TIBIAL COMPRESSION NAIL
Search all 288 clearances from Howmedica Osteonics Corp. →