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FDA 510(k)

PMT Facet Fixation System (PMT FFS)

K-Number: K220951 · 2022-12-09

ApplicantProvidence Medical Technology, Inc.
Decision Date2022-12-09
Product CodeMRW
DecisionSubstantially Equivalent

Device Summary

PMT Facet Fixation System (PMT FFS) is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2022-12-09 under approval number K220951. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT Facet Fixation System (PMT FFS)?

PMT Facet Fixation System (PMT FFS) is a medical device that received FDA 510(k) clearance on 2022-12-09. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K220951.

When was PMT Facet Fixation System (PMT FFS) approved by the FDA?

PMT Facet Fixation System (PMT FFS) received FDA 510(k) clearance on 2022-12-09, under approval number K220951.

What company makes PMT Facet Fixation System (PMT FFS)?

PMT Facet Fixation System (PMT FFS) is manufactured by Providence Medical Technology, Inc..

What is the FDA product code for PMT Facet Fixation System (PMT FFS)?

The FDA product code for PMT Facet Fixation System (PMT FFS) is MRW.

Related Clinical Trials

NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT07277946 AtraUmatic Laparoscopic HerNia Repair Clinical Investigation to Evaluate the Safety and Performance of The ECLIPSIUM System for Mesh Fixation IDE RECRUITING NCT05762055 Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology ENROLLING_BY_INVITATION NCT07245719 Stryker Universal Midface and Upper-Face Fixation System: A Retrospective Post Market Follow Up COMPLETED NCT07485829 Zimmer Biomet-RibFix Titan RECRUITING NCT06720948 The ION Facet Screw System Ambispective Evaluation ENROLLING_BY_INVITATION

Other Devices by Providence Medical Technology, Inc.

K161642CAVUX™ Cervical Cage K172279PMT Posterior Fixation System K170698ALLY(TM) Bone Screws K163474CAVUX CervicalCage-L SA System K163374ALLY™ Facet Screws K180876DTRAX Spinal System

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Related Devices (Code: MRW)

K161798FacetBRIDGE® SystemLdr Spine USA, Inc. K152137FacetBRIDGE SystemLdr Spine USA K163374ALLY™ Facet ScrewsProvidence Medical Technology, Inc. K180729FaSet Fixation SystemHuvexel Co. , Ltd. K173198Facet Screw Fixation SystemU&I Corporation K192744CORRIDOR Fixation SystemGlobus Medical, 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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