RRIANGLE KNIFE

Arthroscope

PHX TECHNOLOGIES CORP.

The following data is part of a premarket notification filed by Phx Technologies Corp. with the FDA for Rriangle Knife.

Pre-market Notification Details

Device IDK954510
510k NumberK954510
Device Name:RRIANGLE KNIFE
ClassificationArthroscope
Applicant PHX TECHNOLOGIES CORP. 1032 SHADY OAKS DR., NO. 100 Denton,  TX  76205
ContactJames F Chapel
CorrespondentJames F Chapel
PHX TECHNOLOGIES CORP. 1032 SHADY OAKS DR., NO. 100 Denton,  TX  76205
Product CodeHRX  
CFR Regulation Number888.1100 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-09-28
Decision Date1995-11-14

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