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FDA 510(k)

CAPSET CALCIUM SULFATE BONE GRAFT PLASTER

K-Number: K955096 · 1996-01-23

ApplicantLifecore Biomedical, Inc.
Decision Date1996-01-23
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAPSET CALCIUM SULFATE 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 1996-01-23 under 510(k) number K955096. 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 CAPSET CALCIUM SULFATE BONE GRAFT PLASTER?

CAPSET CALCIUM SULFATE BONE GRAFT PLASTER is a medical device that received FDA 510(k) clearance on 1996-01-23. The listed applicant is Lifecore Biomedical, Inc.. The 510(k) number is K955096.

When did CAPSET CALCIUM SULFATE BONE GRAFT PLASTER receive FDA 510(k) clearance?

CAPSET CALCIUM SULFATE BONE GRAFT PLASTER received FDA 510(k) clearance on 1996-01-23, under 510(k) number K955096.

Who is the listed applicant for CAPSET CALCIUM SULFATE 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 CAPSET CALCIUM SULFATE BONE GRAFT PLASTER?

The FDA product code for CAPSET CALCIUM SULFATE BONE GRAFT PLASTER is LYC.

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Other records listing Lifecore Biomedical, Inc. as applicant

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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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