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FDA 510(k)

AESCULAP ABSORBABLE CRANIOFIX

K-Number: K040080 · 2004-03-31

ApplicantAesculap, Inc.
Decision Date2004-03-31
Product CodeGXR
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP ABSORBABLE CRANIOFIX is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2004-03-31 under 510(k) number K040080. The device is classified under product code GXR. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP ABSORBABLE CRANIOFIX?

AESCULAP ABSORBABLE CRANIOFIX is a medical device that received FDA 510(k) clearance on 2004-03-31. The listed applicant is Aesculap, Inc.. The 510(k) number is K040080.

When did AESCULAP ABSORBABLE CRANIOFIX receive FDA 510(k) clearance?

AESCULAP ABSORBABLE CRANIOFIX received FDA 510(k) clearance on 2004-03-31, under 510(k) number K040080.

Who is the listed applicant for AESCULAP ABSORBABLE CRANIOFIX?

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

What is the FDA product code for AESCULAP ABSORBABLE CRANIOFIX?

The FDA product code for AESCULAP ABSORBABLE CRANIOFIX is GXR.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: GXR)

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.

K253447Montage Flowable Settable, Resorbable Bone Paste (Burr Hole Cover)Orthocon, Inc.K240137Cranial LOOP, Cranial LOOP L and Cranial LOOP XL Cranial Bone Fixation SystemNeos Surgery S.LK221606Absorbable Cranial Flap Fixation SystemChendu Medart Medical Scientific Co., Ltd.K192310Flap Fixator, Burr Hole CoverOssaware Biotech Co., Ltd.K192162NeuroVention Cranial Fixation System, NuCrani Plates, KTC Burr Hole Cover, DC PlateNeurovention, LLCK181539OSSDSIGN CranioplugOssdsign AB

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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