STRYKER PRESSURE SENSING CANNULA

Arthroscope

Stryker Endoscopy

The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Stryker Pressure Sensing Cannula.

Pre-market Notification Details

Device IDK944593
510k NumberK944593
Device Name:STRYKER PRESSURE SENSING CANNULA
ClassificationArthroscope
Applicant Stryker Endoscopy 2590 WALSH AVE. Santa Clara,  CA  95051 -4085
ContactChristina Vance
CorrespondentChristina Vance
Stryker Endoscopy 2590 WALSH AVE. Santa Clara,  CA  95051 -4085
Product CodeHRX  
CFR Regulation Number888.1100 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1994-09-19
Decision Date1995-09-01

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