FDA 510(k)

Posterior Spine Truss System (PSTS) Interbody Fusion Device

K-Nummer: K171351 · 2017-09-08

Entscheidungsdatum2017-09-08

ProduktcodeMAX

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

Posterior Spine Truss System (PSTS) Interbody Fusion Device is the device name listed in this FDA 510(k) record. The listed applicant is 4Web, Inc.. It received FDA 510(k) clearance on 2017-09-08 under 510(k) number K171351. 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 Posterior Spine Truss System (PSTS) Interbody Fusion Device?

Posterior Spine Truss System (PSTS) Interbody Fusion Device is a medical device that received FDA 510(k) clearance on 2017-09-08. The listed applicant is 4Web, Inc.. The 510(k) number is K171351.

When did Posterior Spine Truss System (PSTS) Interbody Fusion Device receive FDA 510(k) clearance?

Posterior Spine Truss System (PSTS) Interbody Fusion Device received FDA 510(k) clearance on 2017-09-08, under 510(k) number K171351.

Who is the listed applicant for Posterior Spine Truss System (PSTS) Interbody Fusion Device?

The FDA 510(k) record lists 4Web, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Posterior Spine Truss System (PSTS) Interbody Fusion Device?

The FDA product code for Posterior Spine Truss System (PSTS) Interbody Fusion Device is MAX.

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Weitere Einträge mit 4Web, Inc. als Antragsteller

K253201Lumbar Spine Truss System - Plating Solution (LSTS-PS)K203065Lumbar Spine Truss System Plating Solution (LSTS-PS)K200002Vorderer Wirbelsäulen-Truss-System – Stand Alone (ASTS-SA) Interbody-Fusion-Gerät K190870Cervical Spinal Truss System-Stand Alone (CSTS-SA)K190926Hammertoe Truss System (HTS)K172294Osteotomy Truss System (OTS)

Alle 11 Geräte anzeigen →

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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