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FDA 510(k)

BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE

K-Number: K873763 · 1987-12-08

ApplicantGeistlich-Pharma
Decision Date1987-12-08
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE is the device name listed in this FDA 510(k) record. The listed applicant is Geistlich-Pharma. It received FDA 510(k) clearance on 1987-12-08 under 510(k) number K873763. 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 - CERAMIC PURE NATURAL HYDROXYAPATITE?

BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE is a medical device that received FDA 510(k) clearance on 1987-12-08. The listed applicant is Geistlich-Pharma. The 510(k) number is K873763.

When did BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE receive FDA 510(k) clearance?

BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE received FDA 510(k) clearance on 1987-12-08, under 510(k) number K873763.

Who is the listed applicant for BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE?

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 - CERAMIC PURE NATURAL HYDROXYAPATITE?

The FDA product code for BIO-OSS - CERAMIC PURE NATURAL HYDROXYAPATITE is LYC.

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Other records listing Geistlich-Pharma as applicant

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Related Devices (Code: LYC)

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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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