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FDA 510(k)

COLLAGEN POWDER

K-Number: K103648 · 2011-09-14

Decision Date2011-09-14
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

COLLAGEN POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Innocoll Pharmaceuticals, Ltd.. It received FDA 510(k) clearance on 2011-09-14 under 510(k) number K103648. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLAGEN POWDER?

COLLAGEN POWDER is a medical device that received FDA 510(k) clearance on 2011-09-14. The listed applicant is Innocoll Pharmaceuticals, Ltd.. The 510(k) number is K103648.

When did COLLAGEN POWDER receive FDA 510(k) clearance?

COLLAGEN POWDER received FDA 510(k) clearance on 2011-09-14, under 510(k) number K103648.

Who is the listed applicant for COLLAGEN POWDER?

The FDA 510(k) record lists Innocoll Pharmaceuticals, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLLAGEN POWDER?

The FDA product code for COLLAGEN POWDER is KGN.

Related Clinical Trials

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.

Other records listing Innocoll Pharmaceuticals, Ltd. 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.

Related Devices (Code: KGN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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