ANCHOR Tissue Retrieval System
K-Number: K172940 · 2017-10-18
ApplicantConmed Corporation
Decision Date2017-10-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
ANCHOR Tissue Retrieval System is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2017-10-18 under approval number K172940. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ANCHOR Tissue Retrieval System?
ANCHOR Tissue Retrieval System is a medical device that received FDA 510(k) clearance on 2017-10-18. It is manufactured by Conmed Corporation. The 510(k) number is K172940.
When was ANCHOR Tissue Retrieval System approved by the FDA?
ANCHOR Tissue Retrieval System received FDA 510(k) clearance on 2017-10-18, under approval number K172940.
What company makes ANCHOR Tissue Retrieval System?
ANCHOR Tissue Retrieval System is manufactured by Conmed Corporation.
What is the FDA product code for ANCHOR Tissue Retrieval System?
The FDA product code for ANCHOR Tissue Retrieval System is GCJ.
Related Clinical Trials
NCT01143454
Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System
RECRUITING
NCT03053791
Deep Brain Stimulation in Patients With Incomplete Spinal Cord Injury for Improvement of Gait
RECRUITING
NCT07608939
Postoperative Pain After Root Canal Treatment Using Different Root Canal Sealers
NOT_YET_RECRUITING
NCT07278869
Applause Study I - Append System Early Feasibility Study
RECRUITING
NCT07489820
Evaluation of the Efficacy of Negative Pressure Wound Therapy on Perineal Healing Following Abdominoperineal Amputation
NOT_YET_RECRUITING
NCT07581977
A Novel Two-Tooth Clip for ESD and EFTR of GIST
RECRUITING
Related PubMed Literature
PMID: 42168293
Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling.
Scientific reports (2026)
PMID: 40942702
Digital Cardiovascular Twins, AI Agents, and Sensor Data: A Narrative Review from System Architecture to Proactive Heart Health.
Sensors (Basel, Switzerland) (2025)
Other Devices by Conmed Corporation
K151229ABC D-FLEX PROBE
K161017True HD 3MOS Camera System
K152969ENHANCE ALLOGRAFT WEDGE INSTRUMENT TRAY
K172671HelixAR Electrosurgical Generator with Argon Beam Coagulation, HelixAR Mobile Pedestal
K171725CuffLink Implant System
K171592CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver
Related Devices (Code: GCJ)
K163102ReliaCatch Specimen Retrieval Bag 10mm; ReliaCatch Specimen Retrieval Bag 12mmCovidien
K160801Well Lead Extraction BagWell Lead Medical Co., Ltd.
K153773Disposal Lens Cleaning SheathOlympus Medical Systems Corp.
K161720Standard ClampStandard Bariatrics
K162445LiVac Retractor SystemLivac Pty, Ltd.
K162584VersaOne Bladeless TrocarCovidien
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.