Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SILMAX CONTOUR CARVING BLOCK IMPLANT

K-Number: K002629 · 2000-11-20

ApplicantPillar Surgical, Inc.
Decision Date2000-11-20
Product CodeJOF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SILMAX CONTOUR CARVING BLOCK 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 2000-11-20 under 510(k) number K002629. The device is classified under product code JOF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILMAX CONTOUR CARVING BLOCK IMPLANT?

SILMAX CONTOUR CARVING BLOCK IMPLANT is a medical device that received FDA 510(k) clearance on 2000-11-20. The listed applicant is Pillar Surgical, Inc.. The 510(k) number is K002629.

When did SILMAX CONTOUR CARVING BLOCK IMPLANT receive FDA 510(k) clearance?

SILMAX CONTOUR CARVING BLOCK IMPLANT received FDA 510(k) clearance on 2000-11-20, under 510(k) number K002629.

Who is the listed applicant for SILMAX CONTOUR CARVING BLOCK 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 SILMAX CONTOUR CARVING BLOCK IMPLANT?

The FDA product code for SILMAX CONTOUR CARVING BLOCK IMPLANT is JOF.

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 IMPLANTK992239PILLAR CHIN IMPLANTK992242PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTSK992240PILLAR MALAR IMPLANT

Related Devices (Code: JOF)

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.

K200532StarPoreAnatomics Pty, Ltd.K171037PoreStar Patient Specific ImplantAnatomics Pty, Ltd.K083621MEDPOR CUSTOMIZED SURGICAL IMPLANTPorex Surgical, Inc.K771727BIOSPONGE RECONSTRUCTION DISCSXomed, Inc.K771726BIOSPONGE STAPES PISTONXomed, 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.

↑