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FDA 510(k)

KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX

K-Number: K091192 · 2009-11-02

ApplicantKensey Nash Corp.
Decision Date2009-11-02
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX 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 2009-11-02 under 510(k) number K091192. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX?

KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX is a medical device that received FDA 510(k) clearance on 2009-11-02. The listed applicant is Kensey Nash Corp.. The 510(k) number is K091192.

When did KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX receive FDA 510(k) clearance?

KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX received FDA 510(k) clearance on 2009-11-02, under 510(k) number K091192.

Who is the listed applicant for KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX?

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 KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX?

The FDA product code for KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX is NPL.

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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 MATRIXK091499MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)K090919KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANEK073519QUICKCAT EXTRACTION CATHETER, MODEL 60090-01K071695KENSEY NASH MACROPORE SHIELDK072384MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE

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Related Devices (Code: NPL)

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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