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FDA 510(k)

MP 719

K-Number: K111524 · 2011-07-22

ApplicantMarine Polymer Technologies, Inc.
Decision Date2011-07-22
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

MP 719 is the device name listed in this FDA 510(k) record. The listed applicant is Marine Polymer Technologies, Inc.. It received FDA 510(k) clearance on 2011-07-22 under 510(k) number K111524. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MP 719?

MP 719 is a medical device that received FDA 510(k) clearance on 2011-07-22. The listed applicant is Marine Polymer Technologies, Inc.. The 510(k) number is K111524.

When did MP 719 receive FDA 510(k) clearance?

MP 719 received FDA 510(k) clearance on 2011-07-22, under 510(k) number K111524.

Who is the listed applicant for MP 719?

The FDA 510(k) record lists Marine Polymer Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MP 719?

The FDA product code for MP 719 is MTJ.

Other records listing Marine Polymer Technologies, Inc. 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.

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Related Devices (Code: MTJ)

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.

K262769Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT)Orthocon, Inc.K261439Permatage Flowable, Settable Hemostatic Bone PasteOrthocon, Inc.K232998Montage- XT Settable, Resorbable Hemostatic Bone PuttyOrthocon, Inc.K213418MONTAGE Settable, Resorbable Hemostatic Bone PuttyOrthocon, Inc.K231386Montage Flowable XRO Settable, Resorbable Hemostatic Bone PasteOrthocon, Inc.K200452Meril-BonewaxM/s. Meril Endo Surgery Private Limited.

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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