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FDA 510(k)

PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS

K-Number: K992242 · 1999-11-22

ApplicantPillar Surgical, Inc.
Decision Date1999-11-22
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Pillar Surgical, Inc.. It received FDA 510(k) clearance on 1999-11-22 under 510(k) number K992242. The device is classified under product code FZE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS?

PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS is a medical device that received FDA 510(k) clearance on 1999-11-22. The listed applicant is Pillar Surgical, Inc.. The 510(k) number is K992242.

When did PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS receive FDA 510(k) clearance?

PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS received FDA 510(k) clearance on 1999-11-22, under 510(k) number K992242.

Who is the listed applicant for PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS?

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

What is the FDA product code for PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS?

The FDA product code for PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS is FZE.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pillar Surgical, Inc. 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.

K002633SILMAX PECTORAL IMPLANTK002629SILMAX CONTOUR CARVING BLOCK IMPLANTK992239PILLAR CHIN IMPLANTK992240PILLAR MALAR IMPLANT

Related Devices (Code: FZE)

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.

K241253Medicon Epiplating SystemCmf Medicon Surgical, Inc.K161548Osseointegrated FixturesSouthern Implants (Pty), Ltd.K090803HANSON MEDICAL FACIAL IMPLANTSHanson Medical, Inc.K090630NOBEL BIOCARE ENDOSSEOUS IMPLANTS (MAXILLOFACIAL INDICATION)Nobel Biocare ABK071018MONARCH NASAL IMPLANTHanson Medical, Inc.K041690MONARCH NASAL IMPLANTHanson 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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