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FDA 510(k)

4060 POROUS HA PARTICULES BII PORE

K-Number: K924286 · 1993-04-14

ApplicantBio-Interfaces, Inc.
Decision Date1993-04-14
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

4060 POROUS HA PARTICULES BII PORE is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Interfaces, Inc.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K924286. 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 4060 POROUS HA PARTICULES BII PORE?

4060 POROUS HA PARTICULES BII PORE is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Bio-Interfaces, Inc.. The 510(k) number is K924286.

When did 4060 POROUS HA PARTICULES BII PORE receive FDA 510(k) clearance?

4060 POROUS HA PARTICULES BII PORE received FDA 510(k) clearance on 1993-04-14, under 510(k) number K924286.

Who is the listed applicant for 4060 POROUS HA PARTICULES BII PORE?

The FDA 510(k) record lists Bio-Interfaces, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 4060 POROUS HA PARTICULES BII PORE?

The FDA product code for 4060 POROUS HA PARTICULES BII PORE is LYC.

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Other records listing Bio-Interfaces, Inc. 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.

K960164BIO-INTERFACES, INC., BIORESORBABLE CALCIUM PHOSPHATE PARTICLES - BII-GRAFT 6140K954763BIO-INTERFACES, INC,. BII-PLASTK950598BIORESORBABLE CALCIUM PHOSPHATE PARTICLES - BLL-GRAFTK950567BIO-APATITE 6140 HA PARTICLESK950511BLL-FIL 6140 PARTICLESK934049BII-PORE(TM) CANAL WALL PROSTHESIS

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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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