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FDA 510(k)

OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40

K-Number: K852742 · 1985-09-26

ApplicantCoors Biomedical Co.
Decision Date1985-09-26
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 is the device name listed in this FDA 510(k) record. The listed applicant is Coors Biomedical Co.. It received FDA 510(k) clearance on 1985-09-26 under 510(k) number K852742. 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 OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40?

OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 is a medical device that received FDA 510(k) clearance on 1985-09-26. The listed applicant is Coors Biomedical Co.. The 510(k) number is K852742.

When did OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 receive FDA 510(k) clearance?

OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 received FDA 510(k) clearance on 1985-09-26, under 510(k) number K852742.

Who is the listed applicant for OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40?

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

What is the FDA product code for OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40?

The FDA product code for OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 is LYC.

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Other records listing Coors Biomedical Co. 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.

K863176ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+K862324OSTEOGRAF/AR AND OSTEOGRAF/AR+K862061OSTEOGRAF/AR+ PERMARIDGE HYDROXYLAPATITE, 18-40K861084OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESHK861083OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESHK810822DENTAL PORCELAIN POWDER

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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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