PMT Posterior Fixation System
K-Number: K172279 · 2017-09-20
ApplicantProvidence Medical Technology, Inc.
Decision Date2017-09-20
Product CodeNKG
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
PMT Posterior Fixation System is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2017-09-20 under approval number K172279. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PMT Posterior Fixation System?
PMT Posterior Fixation System is a medical device that received FDA 510(k) clearance on 2017-09-20. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K172279.
When was PMT Posterior Fixation System approved by the FDA?
PMT Posterior Fixation System received FDA 510(k) clearance on 2017-09-20, under approval number K172279.
What company makes PMT Posterior Fixation System?
PMT Posterior Fixation System is manufactured by Providence Medical Technology, Inc..
What is the FDA product code for PMT Posterior Fixation System?
The FDA product code for PMT Posterior Fixation System is NKG.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.