FDA 510(k)

ACE WIRE TENSION CLAMP

K-Number: K894982 · 1990-01-11

Decision Date1990-01-11

Product CodeJEC

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ACE WIRE TENSION CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K894982. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE WIRE TENSION CLAMP?

ACE WIRE TENSION CLAMP is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Buckman Co., Inc.. The 510(k) number is K894982.

When did ACE WIRE TENSION CLAMP receive FDA 510(k) clearance?

ACE WIRE TENSION CLAMP received FDA 510(k) clearance on 1990-01-11, under 510(k) number K894982.

Who is the listed applicant for ACE WIRE TENSION CLAMP?

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

What is the FDA product code for ACE WIRE TENSION CLAMP?

The FDA product code for ACE WIRE TENSION CLAMP is JEC.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Buckman Co., Inc. as applicant

K961320CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEM K974641FUTURELASE 3000/3002 ERBIUM LASER SYSTEM K964252ORTHOCHUCK K950099SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM K960451WEBB-MORLEY SPINE SYSTEM K950999KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

View all 111 devices →

Related Devices (Code: JEC)

K203605SteriTrakArbutus Medical, Inc.K193256Anjon Bremer Halo SystemAnjon Holdings, LLC K192465DigiFix Sterile KitVirak Orthopedics, LLC K181192PIP FixHand Biomechanics Lab, Inc.K171863Anjon Bremer Halo SystemAnjon Holdings, LLC K163028Medline ReNewal Reprocessed Stryker External Fixation DevicesSurgical Instrument Service and Savings, 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.