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FDA 510(k)

KENSEY NASH BONE VOID FILLER

K-Number: K060917 · 2006-09-22

ApplicantKensey Nash Corporation
Decision Date2006-09-22
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KENSEY NASH BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Kensey Nash Corporation. It received FDA 510(k) clearance on 2006-09-22 under 510(k) number K060917. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENSEY NASH BONE VOID FILLER?

KENSEY NASH BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2006-09-22. The listed applicant is Kensey Nash Corporation. The 510(k) number is K060917.

When did KENSEY NASH BONE VOID FILLER receive FDA 510(k) clearance?

KENSEY NASH BONE VOID FILLER received FDA 510(k) clearance on 2006-09-22, under 510(k) number K060917.

Who is the listed applicant for KENSEY NASH BONE VOID FILLER?

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

What is the FDA product code for KENSEY NASH BONE VOID FILLER?

The FDA product code for KENSEY NASH BONE VOID FILLER is MQV.

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Other records listing Kensey Nash Corporation 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.

K121310MESOTHELIUM DENTAL MEMBRANEK112888MESO WOUND MATRIXK094061KENSEY NASH ECM SURGICAL PATCHK073162SAFE-CROSS(R) RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM, SAFE-CROSS(R) RADIO FREQUENCY TOTAL OCCLUSION CROSSINGK061030BIOBLANKET SURGICAL MESH

Related Devices (Code: MQV)

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.

K262230Mg OSTEOREVIVE™;Mg OSTEOCRETE™Bone Solutions, Inc.K260364Device 300419 StripGeistlich Pharma AGK252797JAZBI™ Resorbable Bone Void FillerSdip Innovations Pty, Ltd.K261008Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft SubstituteStryker SpineK253524Adaptos®Fuse Bone GraftBiomendex OYK253147FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft SubstituteProsidyan, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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