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FDA 510(k)

PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR

K-Number: K102326 · 2010-11-15

Decision Date2010-11-15
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Parcus Medical, LLC. It received FDA 510(k) clearance on 2010-11-15 under 510(k) number K102326. 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 PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR?

PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR is a medical device that received FDA 510(k) clearance on 2010-11-15. The listed applicant is Parcus Medical, LLC. The 510(k) number is K102326.

When did PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR receive FDA 510(k) clearance?

PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR received FDA 510(k) clearance on 2010-11-15, under 510(k) number K102326.

Who is the listed applicant for PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR?

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

What is the FDA product code for PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR?

The FDA product code for PARCUS 3.5MM PEEK CF PUSH-IN SUTURE ANCHOR is HWC. This falls under the Cardiovascular category.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Parcus Medical, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 26 devices →

Related Devices (Code: HWC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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