Codman Disposable Perforators
K-Number: K183581 · 2019-01-20
ApplicantIntegra Lifesciences Corp.
Decision Date2019-01-20
Product CodeHBF
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Codman Disposable Perforators is a medical device manufactured by Integra Lifesciences Corp.. It received FDA 510(k) clearance on 2019-01-20 under approval number K183581. The device is classified under product code HBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Codman Disposable Perforators?
Codman Disposable Perforators is a medical device that received FDA 510(k) clearance on 2019-01-20. It is manufactured by Integra Lifesciences Corp.. The 510(k) number is K183581.
When was Codman Disposable Perforators approved by the FDA?
Codman Disposable Perforators received FDA 510(k) clearance on 2019-01-20, under approval number K183581.
What company makes Codman Disposable Perforators?
Codman Disposable Perforators is manufactured by Integra Lifesciences Corp..
What is the FDA product code for Codman Disposable Perforators?
The FDA product code for Codman Disposable Perforators is HBF.
Other Devices by Integra Lifesciences Corp.
Related Devices (Code: HBF)
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.