FDA 510(k)

KMTI S141 Lumbar Interbody Fusion System

K-Nummer: K212070 · 2021-08-30

AntragstellerKyocera Medical Technologies, Inc.

Entscheidungsdatum2021-08-30

ProduktcodeMAX

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

KMTI S141 Lumbar Interbody Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is Kyocera Medical Technologies, Inc.. It received FDA 510(k) clearance on 2021-08-30 under 510(k) number K212070. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the KMTI S141 Lumbar Interbody Fusion System?

KMTI S141 Lumbar Interbody Fusion System is a medical device that received FDA 510(k) clearance on 2021-08-30. The listed applicant is Kyocera Medical Technologies, Inc.. The 510(k) number is K212070.

When did KMTI S141 Lumbar Interbody Fusion System receive FDA 510(k) clearance?

KMTI S141 Lumbar Interbody Fusion System received FDA 510(k) clearance on 2021-08-30, under 510(k) number K212070.

Who is the listed applicant for KMTI S141 Lumbar Interbody Fusion System?

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

What is the FDA product code for KMTI S141 Lumbar Interbody Fusion System?

The FDA product code for KMTI S141 Lumbar Interbody Fusion System is MAX.

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Weitere Einträge mit Kyocera Medical Technologies, Inc. als Antragsteller

K261353Tesera-K Anterior Lumbar Interbody Fusion (ALIF) System; Tesera-K XL System; Lumbar Anchor System K242928Tesera-k SC System K242045Initia T3 Acetabular Hemispherical Shell System K242771Tesera-k PL System and Tesera-k XL System K243295Initia Knee System K243015Skyway Anterior Cervical Plate System

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Verwandte Geräte (Code: MAX)

K261049SCALA® TLSpineart SA K261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SystemSeaSpine Orthopedics Corporation K253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.

Offizielle Quelle

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