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FDA 510(k)

MEMOMETAL BONE ANCHORS

K-Number: K071941 · 2007-12-04

ApplicantMemometal Technologies
Decision Date2007-12-04
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMOMETAL BONE ANCHORS is the device name listed in this FDA 510(k) record. The listed applicant is Memometal Technologies. It received FDA 510(k) clearance on 2007-12-04 under 510(k) number K071941. 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 MEMOMETAL BONE ANCHORS?

MEMOMETAL BONE ANCHORS is a medical device that received FDA 510(k) clearance on 2007-12-04. The listed applicant is Memometal Technologies. The 510(k) number is K071941.

When did MEMOMETAL BONE ANCHORS receive FDA 510(k) clearance?

MEMOMETAL BONE ANCHORS received FDA 510(k) clearance on 2007-12-04, under 510(k) number K071941.

Who is the listed applicant for MEMOMETAL BONE ANCHORS?

The FDA 510(k) record lists Memometal Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEMOMETAL BONE ANCHORS?

The FDA product code for MEMOMETAL BONE ANCHORS is HWC. This falls under the Cardiovascular category.

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Other records listing Memometal Technologies 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.

K112197MEMOMETAL INTRA-MEDULLARY BONE FASTENERK101930MEMOMETAL NAVIS BONE PLATING SYSTEMK102072MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)K093820SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115K083447MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50K070598MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE

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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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