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FDA 510(k)

PILLAR MALAR IMPLANT

K-Number: K992240 · 1999-11-22

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

Device Summary

PILLAR MALAR IMPLANT 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 K992240. The device is classified under product code LZK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLAR MALAR IMPLANT?

PILLAR MALAR IMPLANT 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 K992240.

When did PILLAR MALAR IMPLANT receive FDA 510(k) clearance?

PILLAR MALAR IMPLANT received FDA 510(k) clearance on 1999-11-22, under 510(k) number K992240.

Who is the listed applicant for PILLAR MALAR IMPLANT?

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 MALAR IMPLANT?

The FDA product code for PILLAR MALAR IMPLANT is LZK.

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 IMPLANTK992242PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS

Related Devices (Code: LZK)

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.

K021419AART MALAR IMPLANTAesthetic and Reconstructive Technologies, Inc.K002886IMPLANTECH COMPOSITE FACIAL IMPLANTS (MALAR, CHIN, AND NASAL)Implantech Associates, Inc.K983756SURGIFORM ANATOMICAL MALARSurgical Technology Laboratories, Inc.K982763SEARE BIOMEDICAL MALAR IMPLANTSSeare Biomedical Corp.K981835SILIMED MALAR IMPLANTSilimed, LLCK980140SPECTRUM DESIGNS MEDIAL MALAR IMPLANTSpectrum Designs, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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