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)

WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS

K-Number: K864340 · 1986-11-24

ApplicantBuckman Co., Inc.
Decision Date1986-11-24
Product Code
DecisionSubstantially Equivalent

Device Summary

WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS 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 1986-11-24 under 510(k) number K864340. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS?

WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1986-11-24. The listed applicant is Buckman Co., Inc.. The 510(k) number is K864340.

When did WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1986-11-24, under 510(k) number K864340.

Who is the listed applicant for WILLIAMS ORTHOPAEDIC SURGICAL INSTRUMENTS?

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

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 Buckman Co., 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.

K961320CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEMK974641FUTURELASE 3000/3002 ERBIUM LASER SYSTEMK964252ORTHOCHUCKK950099SYNERGY(TM) TI POSTERIOR SPINAL SYSTEMK960451WEBB-MORLEY SPINE SYSTEMK950999KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

View all 111 devices →

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.

↑