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FDA 510(k)

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER

K-Number: K910432 · 1991-05-01

ApplicantLifecore Biomedical, Inc.
Decision Date1991-05-01
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER is the device name listed in this FDA 510(k) record. The listed applicant is Lifecore Biomedical, Inc.. It received FDA 510(k) clearance on 1991-05-01 under 510(k) number K910432. 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 HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER?

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER is a medical device that received FDA 510(k) clearance on 1991-05-01. The listed applicant is Lifecore Biomedical, Inc.. The 510(k) number is K910432.

When did HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER receive FDA 510(k) clearance?

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER received FDA 510(k) clearance on 1991-05-01, under 510(k) number K910432.

Who is the listed applicant for HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER?

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

What is the FDA product code for HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER?

The FDA product code for HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER is LYC.

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Other records listing Lifecore Biomedical, 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.

K073032PRIMACONNEX SD ESTHETIC CONTOUR ZI ABUTMENTSK072241PRIMACONNEX CAD/CAM ABUTMENT SYSTEMK072768RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTSK072572PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTSK062876PRIMACONNEX CERAMIC ABUTMENTSK060530SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.

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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.

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