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)

KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE

K-Number: K060414 · 2006-10-23

ApplicantKmi Kolster Methods, Inc.
Decision Date2006-10-23
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Kmi Kolster Methods, Inc.. It received FDA 510(k) clearance on 2006-10-23 under 510(k) number K060414. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE?

KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE is a medical device that received FDA 510(k) clearance on 2006-10-23. The listed applicant is Kmi Kolster Methods, Inc.. The 510(k) number is K060414.

When did KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE receive FDA 510(k) clearance?

KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE received FDA 510(k) clearance on 2006-10-23, under 510(k) number K060414.

Who is the listed applicant for KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE?

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

What is the FDA product code for KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE?

The FDA product code for KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE is GAW.

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 Kmi Kolster Methods, 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.

K043591FEATHERLIFT EXTENDED APTOS THREADK012236STARS2000 POWER CANNULAK010702XUB EXTERNAL ULTRASOUNDK002859SSW-STERILE SOLUTION WARMERK991203IRRIGATION OR INFUSION PUMP K PUMP

Related Devices (Code: GAW)

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.

K253572STRATAFIX™ Spiral PRONOVA™ Unidirectional Knotless Tissue Control Device STRATAFIX™ Spiral PRONOVA™ Bidirectional Knotless Tissue Control DeviceETHICON, Inc.K233355Cypris eXact Suturing SystemCypris MedicalK230746Non absorbable Surgical Polypropylene SutureShandong Haidike Medical Products Co., Ltd.K221280VessealLydus Medical , Ltd.K211178DURAMESH Mesh SutureMsiK192953APTOS Threads – Polypropylene Surgical SuturesAptos, LLC

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.

↑