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FDA 510(k)

CYPRESS MEDICAL BONE SCREW & PLATES

K-Number: K894719 · 1989-10-20

ApplicantCypress Medical Mfg., Inc.
Decision Date1989-10-20
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CYPRESS MEDICAL BONE SCREW & PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Cypress Medical Mfg., Inc.. It received FDA 510(k) clearance on 1989-10-20 under 510(k) number K894719. 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 CYPRESS MEDICAL BONE SCREW & PLATES?

CYPRESS MEDICAL BONE SCREW & PLATES is a medical device that received FDA 510(k) clearance on 1989-10-20. The listed applicant is Cypress Medical Mfg., Inc.. The 510(k) number is K894719.

When did CYPRESS MEDICAL BONE SCREW & PLATES receive FDA 510(k) clearance?

CYPRESS MEDICAL BONE SCREW & PLATES received FDA 510(k) clearance on 1989-10-20, under 510(k) number K894719.

Who is the listed applicant for CYPRESS MEDICAL BONE SCREW & PLATES?

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

What is the FDA product code for CYPRESS MEDICAL BONE SCREW & PLATES?

The FDA product code for CYPRESS MEDICAL BONE SCREW & PLATES is HWC. This falls under the Cardiovascular category.

Related Clinical Trials

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Other records listing Cypress Medical Mfg., Inc. 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.

K894830CYPRESS CANNULATED BONE SCREW

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.

K262975Arthrex Beaming SystemArthrex, Inc.K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps OrthoK261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower OrthopedK262344Large Compression ScrewsTriMed, Inc.

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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