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FDA 510(k)

MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)

K-Number: K102072 · 2010-11-03

ApplicantMemometal Technologies
Decision Date2010-11-03
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) is the device name listed in this FDA 510(k) record. The listed applicant is Memometal Technologies. It received FDA 510(k) clearance on 2010-11-03 under 510(k) number K102072. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)?

MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) is a medical device that received FDA 510(k) clearance on 2010-11-03. The listed applicant is Memometal Technologies. The 510(k) number is K102072.

When did MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) receive FDA 510(k) clearance?

MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) received FDA 510(k) clearance on 2010-11-03, under 510(k) number K102072.

Who is the listed applicant for MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)?

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 IMPLANTS (K-SNAP & TI-FUSE)?

The FDA product code for MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) is HTY.

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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 SYSTEMK093820SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115K083447MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50K071941MEMOMETAL BONE ANCHORSK070598MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE

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Related Devices (Code: HTY)

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.

K262722Primal K-Wire (P99-193-1410)Paragon 28, Inc.K253325ZipToe™ Hammertoe Fusion SystemToetal SolutionsK252657Impact PEEK Union Nail SystemNvision Biomedical Technologies, Inc.K250315RONAVIS – FX (FX-001)AIRS, Inc.K251362PediFlex™ Flexible Nail SystemOrthoPediatrics Corp.K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies

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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