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FDA 510(k)

INTERPORE 200 POROUS HYDROXYAPATITE

K-Number: K860983 · 1986-05-23

ApplicantInterpore Intl.
Decision Date1986-05-23
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE 200 POROUS HYDROXYAPATITE is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1986-05-23 under 510(k) number K860983. 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 INTERPORE 200 POROUS HYDROXYAPATITE?

INTERPORE 200 POROUS HYDROXYAPATITE is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is Interpore Intl.. The 510(k) number is K860983.

When did INTERPORE 200 POROUS HYDROXYAPATITE receive FDA 510(k) clearance?

INTERPORE 200 POROUS HYDROXYAPATITE received FDA 510(k) clearance on 1986-05-23, under 510(k) number K860983.

Who is the listed applicant for INTERPORE 200 POROUS HYDROXYAPATITE?

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

What is the FDA product code for INTERPORE 200 POROUS HYDROXYAPATITE?

The FDA product code for INTERPORE 200 POROUS HYDROXYAPATITE is LYC.

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Other records listing Interpore Intl. 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.

K981253ULTRACON ULTRAFILTRATORK980817PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30LK972842INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGEK971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEK960945IMZ MEMBRANE TACK SYSTEMK960371INTERPORE THREADED IMPLANT

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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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