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FDA 510(k)

COPIOS BONE VOID FILLER SPONGE AND PASTE

K-Number: K071237 · 2007-06-01

ApplicantKensey Nash Corp.
Decision Date2007-06-01
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COPIOS BONE VOID FILLER SPONGE AND PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Kensey Nash Corp.. It received FDA 510(k) clearance on 2007-06-01 under 510(k) number K071237. 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 COPIOS BONE VOID FILLER SPONGE AND PASTE?

COPIOS BONE VOID FILLER SPONGE AND PASTE is a medical device that received FDA 510(k) clearance on 2007-06-01. The listed applicant is Kensey Nash Corp.. The 510(k) number is K071237.

When did COPIOS BONE VOID FILLER SPONGE AND PASTE receive FDA 510(k) clearance?

COPIOS BONE VOID FILLER SPONGE AND PASTE received FDA 510(k) clearance on 2007-06-01, under 510(k) number K071237.

Who is the listed applicant for COPIOS BONE VOID FILLER SPONGE AND PASTE?

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

What is the FDA product code for COPIOS BONE VOID FILLER SPONGE AND PASTE?

The FDA product code for COPIOS BONE VOID FILLER SPONGE AND PASTE is MQV.

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Other records listing Kensey Nash Corp. 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.

K103787MEDEOR MATRIXK091192KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XXK091499MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)K090919KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANEK073519QUICKCAT EXTRACTION CATHETER, MODEL 60090-01K071695KENSEY NASH MACROPORE SHIELD

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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

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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