FIBULA PLATE PROLOCK WITH ANGULAR STABILITY

Plate, Fixation, Bone

I.T.S. IMPLANTAT-TECHNOLOGIE-SYSTEME GMBH

The following data is part of a premarket notification filed by I.t.s. Implantat-technologie-systeme Gmbh with the FDA for Fibula Plate Prolock With Angular Stability.

Pre-market Notification Details

Device IDK063672
510k NumberK063672
Device Name:FIBULA PLATE PROLOCK WITH ANGULAR STABILITY
ClassificationPlate, Fixation, Bone
Applicant I.T.S. IMPLANTAT-TECHNOLOGIE-SYSTEME GMBH 3150 E. 200TH ST. Prior Lake,  MN  55372
ContactAl Lippincott
CorrespondentAl Lippincott
I.T.S. IMPLANTAT-TECHNOLOGIE-SYSTEME GMBH 3150 E. 200TH ST. Prior Lake,  MN  55372
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-12-11
Decision Date2007-02-02
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
09120047307281 K063672 000
09120047298336 K063672 000
09120047298329 K063672 000
09120047298312 K063672 000
09120047298305 K063672 000
09120047298299 K063672 000
09120047298282 K063672 000
09120047298275 K063672 000
09120047298268 K063672 000
09120034302671 K063672 000
09120034302664 K063672 000
09120034302657 K063672 000
09120034302640 K063672 000
09120034302633 K063672 000
09120034302626 K063672 000
09120047298343 K063672 000
09120047298350 K063672 000
09120047306925 K063672 000
09120047307274 K063672 000
09120047307267 K063672 000
09120047307250 K063672 000
09120047307243 K063672 000
09120047307236 K063672 000
09120047307229 K063672 000
09120047307151 K063672 000
09120047307144 K063672 000
09120047307137 K063672 000
09120047307120 K063672 000
09120047307113 K063672 000
09120047307106 K063672 000
09120047307090 K063672 000
09120047306932 K063672 000
09120069817089 K063672 000

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.