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FDA 510(k)

BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN

K-Number: K033815 · 2004-01-15

ApplicantGeistlich-Pharma
Decision Date2004-01-15
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN is the device name listed in this FDA 510(k) record. The listed applicant is Geistlich-Pharma. It received FDA 510(k) clearance on 2004-01-15 under 510(k) number K033815. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN?

BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN is a medical device that received FDA 510(k) clearance on 2004-01-15. The listed applicant is Geistlich-Pharma. The 510(k) number is K033815.

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

BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN received FDA 510(k) clearance on 2004-01-15, under 510(k) number K033815.

Who is the listed applicant for BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN?

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, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN?

The FDA product code for BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN is NPM.

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Other records listing Geistlich-Pharma as applicant

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Related Devices (Code: NPM)

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.

K254210REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)Hyundai Bioland Co., Ltd.K253723BOSSMedpark Co., Ltd.K251786Geistlich Bio-Oss®; Geistlich Bio-Oss Pen®Geistlich Pharma AGK251613SwissGraft XGeistlich Pharma AGK242510Geistlich Bio-Flow®Geistlich Pharma AGK240133Xenograft Bovine Bone ParticulateCollagen Solutions, LLC

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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