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FDA 510(k)

MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER

K-Number: K073054 · 2007-11-27

ApplicantCayenne Medical, Inc.
Decision Date2007-11-27
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER is the device name listed in this FDA 510(k) record. The listed applicant is Cayenne Medical, Inc.. It received FDA 510(k) clearance on 2007-11-27 under 510(k) number K073054. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER?

MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER is a medical device that received FDA 510(k) clearance on 2007-11-27. The listed applicant is Cayenne Medical, Inc.. The 510(k) number is K073054.

When did MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER receive FDA 510(k) clearance?

MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER received FDA 510(k) clearance on 2007-11-27, under 510(k) number K073054.

Who is the listed applicant for MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER?

The FDA 510(k) record lists Cayenne Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER?

The FDA product code for MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER is HWC. This falls under the Cardiovascular category.

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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.

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