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)

ANTERIOR ALVEOLAR RIDGE SIZER

K-Number: K843153 · 1984-09-27

ApplicantInterpore Intl.
Decision Date1984-09-27
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANTERIOR ALVEOLAR RIDGE SIZER is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1984-09-27 under 510(k) number K843153. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTERIOR ALVEOLAR RIDGE SIZER?

ANTERIOR ALVEOLAR RIDGE SIZER is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Interpore Intl.. The 510(k) number is K843153.

When did ANTERIOR ALVEOLAR RIDGE SIZER receive FDA 510(k) clearance?

ANTERIOR ALVEOLAR RIDGE SIZER received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843153.

Who is the listed applicant for ANTERIOR ALVEOLAR RIDGE SIZER?

The FDA 510(k) record lists Interpore Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANTERIOR ALVEOLAR RIDGE SIZER?

The FDA product code for ANTERIOR ALVEOLAR RIDGE SIZER is LYC.

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 Interpore Intl. 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.

K981253ULTRACON ULTRAFILTRATORK980817PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30LK972842INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGEK971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEK960945IMZ MEMBRANE TACK SYSTEMK960371INTERPORE THREADED IMPLANT

View all 25 devices →

Related Devices (Code: LYC)

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.

K253317Cytrans™ ElashieldGC America, Inc.K253883Bonalive MaxillofacialBonalive , Ltd.K251818BONTREE PLUSHudens Bio Co., Ltd.K244006FG Bone Graft MFull Golden Biotech Co., Ltd.K243745FG Bone Graft BFull Golden Biotech CorporationK241186Synthetic Bone Graft ParticulateShenzhen Dazhou Medical Technology Co., 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.

↑