FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

STRYKER SPINE OASYS BONE SCREW

K Number: K031657 · Decision Aug 22, 2003
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
288
Review Days
86

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Basic Information

Device Name
STRYKER SPINE OASYS BONE SCREW
K Number
K031657
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics Corp.
Date Received
May 28, 2003
Decision Date
August 22, 2003
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

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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
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