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

STRYKER ORTHOPAEDICS RFID INSTRUMENTATION

K Number: K053348 · Decision Aug 4, 2006
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
288
Review Days
245

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Basic Information

Device Name
STRYKER ORTHOPAEDICS RFID INSTRUMENTATION
K Number
K053348
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics Corp.
Date Received
December 2, 2005
Decision Date
August 4, 2006
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

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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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