THERMO-PLASTIC SHAVER BLADES

Arthroscope

Stryker Endoscopy

The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Thermo-plastic Shaver Blades.

Pre-market Notification Details

Device IDK963332
510k NumberK963332
Device Name:THERMO-PLASTIC SHAVER BLADES
ClassificationArthroscope
Applicant Stryker Endoscopy 2590 WALSH AVE. Santa Clara,  CA  95051 -4085
ContactEric Finley
CorrespondentEric Finley
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 Received1996-08-23
Decision Date1996-10-11
Summary:summary

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.