WARSAW ORTHOPEDIC CANCELLOUS BONE SCREW

Screw, Fixation, Bone

BUCKMAN CO., INC.

The following data is part of a premarket notification filed by Buckman Co., Inc. with the FDA for Warsaw Orthopedic Cancellous Bone Screw.

Pre-market Notification Details

Device IDK862230
510k NumberK862230
Device Name:WARSAW ORTHOPEDIC CANCELLOUS BONE SCREW
ClassificationScrew, Fixation, Bone
Applicant BUCKMAN CO., INC. 921 CALLE VERDE Martinez,  CA  94553
ContactPamela M Buckman
CorrespondentPamela M Buckman
BUCKMAN CO., INC. 921 CALLE VERDE Martinez,  CA  94553
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-06-11
Decision Date1986-08-29

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