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)

SURCAN KNEE HOLDING DEVICE

K-Number: K802558 · 1980-10-31

ApplicantBend Orthopedic & Fracture Clinic
Decision Date1980-10-31
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURCAN KNEE HOLDING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Bend Orthopedic & Fracture Clinic. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802558. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURCAN KNEE HOLDING DEVICE?

SURCAN KNEE HOLDING DEVICE is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Bend Orthopedic & Fracture Clinic. The 510(k) number is K802558.

When did SURCAN KNEE HOLDING DEVICE receive FDA 510(k) clearance?

SURCAN KNEE HOLDING DEVICE received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802558.

Who is the listed applicant for SURCAN KNEE HOLDING DEVICE?

The FDA 510(k) record lists Bend Orthopedic & Fracture Clinic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURCAN KNEE HOLDING DEVICE?

The FDA product code for SURCAN KNEE HOLDING DEVICE is FWZ.

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

Related Devices (Code: FWZ)

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.

K960019RETRACTOR ARM CLAMPBiopsys Medical, Inc.K945415'LIL MAC ACCESSORY CLAMP(TM)D.L. Nelson and Assoc., Inc.K944779CARBON LIGHTS HAND SURGERY TABLEAllen Medical Systems, Inc.K935381KAPS POSITIONING ARMAndronic Devices, Ltd.K931037WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)Whitmore Ent., Inc.K926225SPONGE COUNTERAmerican Medical Manufacturer, 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.

↑