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FDA 510(k)

TITANIUM CANNULATED INTERFERENCE SCREW

K-Number: K021030 · 2002-06-25

ApplicantFuture Medical Systems, Inc.
Decision Date2002-06-25
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM CANNULATED INTERFERENCE SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Future Medical Systems, Inc.. It received FDA 510(k) clearance on 2002-06-25 under 510(k) number K021030. 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 TITANIUM CANNULATED INTERFERENCE SCREW?

TITANIUM CANNULATED INTERFERENCE SCREW is a medical device that received FDA 510(k) clearance on 2002-06-25. The listed applicant is Future Medical Systems, Inc.. The 510(k) number is K021030.

When did TITANIUM CANNULATED INTERFERENCE SCREW receive FDA 510(k) clearance?

TITANIUM CANNULATED INTERFERENCE SCREW received FDA 510(k) clearance on 2002-06-25, under 510(k) number K021030.

Who is the listed applicant for TITANIUM CANNULATED INTERFERENCE SCREW?

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

What is the FDA product code for TITANIUM CANNULATED INTERFERENCE SCREW?

The FDA product code for TITANIUM CANNULATED INTERFERENCE SCREW is HWC. This falls under the Cardiovascular category.

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Other records listing Future Medical Systems, 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.

K023963ADHOC CLAWK013685PLLA CANNULATED INTERFERENCE SCREWK002040FMS SOLOK980808ENDO FMS UROLOGYK955500FMS ARTHOPROBEK954465FMS DUO

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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

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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