RAYLOR(TM) PERIOSTEAL ELEVATORS

Elevator, Surgical, General & Plastic Surgery

CEDAR SURGICAL, INC.

The following data is part of a premarket notification filed by Cedar Surgical, Inc. with the FDA for Raylor(tm) Periosteal Elevators.

Pre-market Notification Details

Device IDK864421
510k NumberK864421
Device Name:RAYLOR(TM) PERIOSTEAL ELEVATORS
ClassificationElevator, Surgical, General & Plastic Surgery
Applicant CEDAR SURGICAL, INC. 15265 MINNETONKA BLVD. Minnetonka,  MN  55345
ContactTerry P Corbin
CorrespondentTerry P Corbin
CEDAR SURGICAL, INC. 15265 MINNETONKA BLVD. Minnetonka,  MN  55345
Product CodeGEG  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-11-10
Decision Date1986-11-26

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