Dunamis PunchTac Suture Anchors
K-Number: K193245 · 2020-02-14
ApplicantDunamis, LLC
Decision Date2020-02-14
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Dunamis PunchTac Suture Anchors is a medical device manufactured by Dunamis, LLC. It received FDA 510(k) clearance on 2020-02-14 under approval number K193245. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Dunamis PunchTac Suture Anchors?
Dunamis PunchTac Suture Anchors is a medical device that received FDA 510(k) clearance on 2020-02-14. It is manufactured by Dunamis, LLC. The 510(k) number is K193245.
When was Dunamis PunchTac Suture Anchors approved by the FDA?
Dunamis PunchTac Suture Anchors received FDA 510(k) clearance on 2020-02-14, under approval number K193245.
What company makes Dunamis PunchTac Suture Anchors?
Dunamis PunchTac Suture Anchors is manufactured by Dunamis, LLC.
What is the FDA product code for Dunamis PunchTac Suture Anchors?
The FDA product code for Dunamis PunchTac Suture Anchors is MBI.
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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.