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FDA 510(k)

MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE

K-Number: K072384 · 2007-09-21

ApplicantKensey Nash Corp.
Decision Date2007-09-21
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & 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 2007-09-21 under 510(k) number K072384. 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 MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE?

MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE is a medical device that received FDA 510(k) clearance on 2007-09-21. The listed applicant is Kensey Nash Corp.. The 510(k) number is K072384.

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

MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE received FDA 510(k) clearance on 2007-09-21, under 510(k) number K072384.

Who is the listed applicant for MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & 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 MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE?

The FDA product code for MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & 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.

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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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