Momentum Posterior Spinal Fixation System
K-Number: K191932 · 2019-10-02
ApplicantUlrich Medical USA
Decision Date2019-10-02
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Momentum Posterior Spinal Fixation System is a medical device manufactured by Ulrich Medical USA. It received FDA 510(k) clearance on 2019-10-02 under approval number K191932. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Momentum Posterior Spinal Fixation System?
Momentum Posterior Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2019-10-02. It is manufactured by Ulrich Medical USA. The 510(k) number is K191932.
When was Momentum Posterior Spinal Fixation System approved by the FDA?
Momentum Posterior Spinal Fixation System received FDA 510(k) clearance on 2019-10-02, under approval number K191932.
What company makes Momentum Posterior Spinal Fixation System?
Momentum Posterior Spinal Fixation System is manufactured by Ulrich Medical USA.
What is the FDA product code for Momentum Posterior Spinal Fixation System?
The FDA product code for Momentum Posterior Spinal Fixation System is NKB.
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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.