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)

PARALLELING GUIDES

K-Number: K914715 · 1994-02-16

ApplicantImplant Corp. of America
Decision Date1994-02-16
Product CodeFZX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PARALLELING GUIDES is the device name listed in this FDA 510(k) record. The listed applicant is Implant Corp. of America. It received FDA 510(k) clearance on 1994-02-16 under 510(k) number K914715. The device is classified under product code FZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARALLELING GUIDES?

PARALLELING GUIDES is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is Implant Corp. of America. The 510(k) number is K914715.

When did PARALLELING GUIDES receive FDA 510(k) clearance?

PARALLELING GUIDES received FDA 510(k) clearance on 1994-02-16, under 510(k) number K914715.

Who is the listed applicant for PARALLELING GUIDES?

The FDA 510(k) record lists Implant Corp. of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARALLELING GUIDES?

The FDA product code for PARALLELING GUIDES is FZX.

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 Implant Corp. of America 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.

K914714BONE DRILLS OR TAPSK914724ADA SHANK EXTENSION

Related Devices (Code: FZX)

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.

K871413CIVCO STEPPERCIVCO Medical Instruments Co., Inc.K871503BIOPSY NEEDLE GUIDE KIT, STERILEAmedic USAK862564A.C.L. GUIDE KITAspen Laboratories, Inc.K854262MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLYMeadox Surgimed, Inc.K852402NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZERNorth American Instrument Corp.K842698BRITISH SPINAL FUSION SETDowns Surgical , Ltd.

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.

↑