ACE/FISCHER PERCUTANEOUS HALF PINS

Pin, Fixation, Threaded

BUCKMAN CO., INC.

The following data is part of a premarket notification filed by Buckman Co., Inc. with the FDA for Ace/fischer Percutaneous Half Pins.

Pre-market Notification Details

Device IDK875012
510k NumberK875012
Device Name:ACE/FISCHER PERCUTANEOUS HALF PINS
ClassificationPin, Fixation, Threaded
Applicant BUCKMAN CO., INC. 921 CALLE VERDE Martinez,  CA  94553
ContactDavid W Schlerf
CorrespondentDavid W Schlerf
BUCKMAN CO., INC. 921 CALLE VERDE Martinez,  CA  94553
Product CodeJDW  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-12-04
Decision Date1988-01-14

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