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FDA 510(k)

SYNOSS SYNTHETIC BONE GRAFT MATERIAL

K-Number: K072397 · 2007-10-18

ApplicantCollagen Matrix, Inc.
Decision Date2007-10-18
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYNOSS SYNTHETIC BONE GRAFT MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2007-10-18 under 510(k) number K072397. 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 SYNOSS SYNTHETIC BONE GRAFT MATERIAL?

SYNOSS SYNTHETIC BONE GRAFT MATERIAL is a medical device that received FDA 510(k) clearance on 2007-10-18. The listed applicant is Collagen Matrix, Inc.. The 510(k) number is K072397.

When did SYNOSS SYNTHETIC BONE GRAFT MATERIAL receive FDA 510(k) clearance?

SYNOSS SYNTHETIC BONE GRAFT MATERIAL received FDA 510(k) clearance on 2007-10-18, under 510(k) number K072397.

Who is the listed applicant for SYNOSS SYNTHETIC BONE GRAFT MATERIAL?

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

What is the FDA product code for SYNOSS SYNTHETIC BONE GRAFT MATERIAL?

The FDA product code for SYNOSS SYNTHETIC BONE GRAFT MATERIAL is LYC.

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Other records listing Collagen Matrix, 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.

K251191Collagen Dura Regeneration Membrane - RepairK243071Bovine Dermis Collagen Dermal MatrixK242302RejuvaKnee™ Collagen Meniscus ImplantK233203Soft Tissue Augmentation Resorbable MatrixK240424Mineral Collagen Composite Bioactive Moldable Bone Graft MatrixK231942Mineral Collagen Composite Bioactive Extra Moldable

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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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