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FDA 510(k)

RESOR-PIN RESORBABLE MEMBRANE PIN

K-Number: K972817 · 1998-07-24

ApplicantGeistlich-Pharma
Decision Date1998-07-24
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RESOR-PIN RESORBABLE MEMBRANE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Geistlich-Pharma. It received FDA 510(k) clearance on 1998-07-24 under 510(k) number K972817. 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 RESOR-PIN RESORBABLE MEMBRANE PIN?

RESOR-PIN RESORBABLE MEMBRANE PIN is a medical device that received FDA 510(k) clearance on 1998-07-24. The listed applicant is Geistlich-Pharma. The 510(k) number is K972817.

When did RESOR-PIN RESORBABLE MEMBRANE PIN receive FDA 510(k) clearance?

RESOR-PIN RESORBABLE MEMBRANE PIN received FDA 510(k) clearance on 1998-07-24, under 510(k) number K972817.

Who is the listed applicant for RESOR-PIN RESORBABLE MEMBRANE PIN?

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 RESOR-PIN RESORBABLE MEMBRANE PIN?

The FDA product code for RESOR-PIN RESORBABLE MEMBRANE PIN 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.

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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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