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FDA 510(k)

Straumann Jason Membrane

K-Number: K173562 · 2018-07-09

ApplicantInstitut Straumann AG
Decision Date2018-07-09
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Straumann Jason Membrane is the device name listed in this FDA 510(k) record. The listed applicant is Institut Straumann AG. It received FDA 510(k) clearance on 2018-07-09 under 510(k) number K173562. 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 Straumann Jason Membrane?

Straumann Jason Membrane is a medical device that received FDA 510(k) clearance on 2018-07-09. The listed applicant is Institut Straumann AG. The 510(k) number is K173562.

When did Straumann Jason Membrane receive FDA 510(k) clearance?

Straumann Jason Membrane received FDA 510(k) clearance on 2018-07-09, under 510(k) number K173562.

Who is the listed applicant for Straumann Jason Membrane?

The FDA 510(k) record lists Institut Straumann AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Straumann Jason Membrane?

The FDA product code for Straumann Jason Membrane is NPL.

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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.

K242817Jason membraneBotiss Biomaterials GmbHK250512Augmented Gingival MatrixNeo Modulus (Suzhou) Medical Sci-Tech Co., Ltd.K252253Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide®Geistlich Pharma AGK251062Geistlich Bio-Gide; Geistlich Bio-Gide® Shape; Geistlich Bio-Gide® Compressed; Geistlich Bio-Gide® Forte; Geistlich Bio-Gide® Perio; Geistlich Combi-Kit Collagen®; Geistlich Perio-System Combi PackGeistlich Pharma AGK250833SwissMembrane X; SwissMembrane X SocketGeistlich Pharma AGK233203Soft Tissue Augmentation Resorbable MatrixCollagen Matrix, 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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