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FDA 510(k)

BIO-OSS BLOCKS

K-Number: K920508 · 1992-11-24

ApplicantGeistlich-Pharma
Decision Date1992-11-24
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIO-OSS BLOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Geistlich-Pharma. It received FDA 510(k) clearance on 1992-11-24 under 510(k) number K920508. 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 BIO-OSS BLOCKS?

BIO-OSS BLOCKS is a medical device that received FDA 510(k) clearance on 1992-11-24. The listed applicant is Geistlich-Pharma. The 510(k) number is K920508.

When did BIO-OSS BLOCKS receive FDA 510(k) clearance?

BIO-OSS BLOCKS received FDA 510(k) clearance on 1992-11-24, under 510(k) number K920508.

Who is the listed applicant for BIO-OSS BLOCKS?

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

What is the FDA product code for BIO-OSS BLOCKS?

The FDA product code for BIO-OSS BLOCKS is LYC.

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Other records listing Geistlich-Pharma 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.

K033815BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGENK014289ORTHOSS RESORBABLE BONE VOID FILLERK970569BIO-BLOCKSK974399BIO-OSS COLLAGENK970321BIO-OSS ANORGANIC BOVINE BONEK972817RESOR-PIN RESORBABLE MEMBRANE PIN

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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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