RANGE SPINAL SYSTEM (MESA AND DENALI)

Orthosis, Spinal Pedicle Fixation

K2M, INC.

The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Range Spinal System (mesa And Denali).

Pre-market Notification Details

Device IDK112920
510k NumberK112920
Device Name:RANGE SPINAL SYSTEM (MESA AND DENALI)
ClassificationOrthosis, Spinal Pedicle Fixation
Applicant K2M, INC. 751 MILLER DR.,SE Leesburg,  VA  20175
ContactNancy Giezen
CorrespondentNancy Giezen
K2M, INC. 751 MILLER DR.,SE Leesburg,  VA  20175
Product CodeMNI  
Subsequent Product CodeKWP
Subsequent Product CodeMNH
CFR Regulation Number888.3070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2011-10-03
Decision Date2011-12-21
Summary:summary

NIH GUDID Devices

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