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)

BIOSORBFX AND BIOSORBPDX MESH

K-Number: K010687 · 2001-03-14

ApplicantBionx Implants, Inc.
Decision Date2001-03-14
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIOSORBFX AND BIOSORBPDX MESH is the device name listed in this FDA 510(k) record. The listed applicant is Bionx Implants, Inc.. It received FDA 510(k) clearance on 2001-03-14 under 510(k) number K010687. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOSORBFX AND BIOSORBPDX MESH?

BIOSORBFX AND BIOSORBPDX MESH is a medical device that received FDA 510(k) clearance on 2001-03-14. The listed applicant is Bionx Implants, Inc.. The 510(k) number is K010687.

When did BIOSORBFX AND BIOSORBPDX MESH receive FDA 510(k) clearance?

BIOSORBFX AND BIOSORBPDX MESH received FDA 510(k) clearance on 2001-03-14, under 510(k) number K010687.

Who is the listed applicant for BIOSORBFX AND BIOSORBPDX MESH?

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

What is the FDA product code for BIOSORBFX AND BIOSORBPDX MESH?

The FDA product code for BIOSORBFX AND BIOSORBPDX MESH is JEY.

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 Bionx Implants, 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.

K023022NUGEN FX SCREWK011569BIOSORBFX O/M 2.0/2/4 SYSTEMK013546MODIFICATION TO: 1.5 BONE FIXATION KIT, MODELS BXS6114, BXS6214K013057BIOCUFF,C, MODELS 236018, 236028, 236036K012334CONTOUR MENISCUS ARROW, MODELS 541110, 541113, AND 541116K010983PLLA PIN

View all 18 devices →

Related Devices (Code: JEY)

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.

K260137KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient SolutionsKLS-Martin L.P.K253206METICULY Patient-specific CMF solutionMeticuly Co., Ltd.K252246Leforte MMF SystemJeil Medical CorporationK253373Southern Craniomaxillofacial (CMF) SystemSouthern Medical (Pty) , Ltd.K251441Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation SystemInion OYK241314KLS Martin Oral-Max Implants MR Conditional (bundled)KLS-Martin L.P.

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.

↑