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

REUNION RSA SHOULDER SYSTEM

K Number: K130895 · Decision Dec 27, 2013
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
288
Review Days
270

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Basic Information

Device Name
REUNION RSA SHOULDER SYSTEM
K Number
K130895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics Corp.
Date Received
April 1, 2013
Decision Date
December 27, 2013
Product Code
PHX
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
PHX Shoulder Prosthesis, Reverse Configuration

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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
K112556 ADM AND ADM/MDM DURATION INSERTS, ADM AND ADM/MDM X3 INSERTS
Search all 288 clearances from Howmedica Osteonics Corp. →