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FDA 510(k)

ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL

K-Number: K873688 · 1987-10-26

ApplicantDentsply Intl.
Decision Date1987-10-26
Product CodeJXH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1987-10-26 under 510(k) number K873688. The device is classified under product code JXH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL?

ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL is a medical device that received FDA 510(k) clearance on 1987-10-26. The listed applicant is Dentsply Intl.. The 510(k) number is K873688.

When did ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL receive FDA 510(k) clearance?

ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL received FDA 510(k) clearance on 1987-10-26, under 510(k) number K873688.

Who is the listed applicant for ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL?

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

What is the FDA product code for ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL?

The FDA product code for ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL is JXH.

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Related Devices (Code: JXH)

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.

K071776ANEUROPLASTIC, MODEL 43-1290Codman & Shurtleff, Inc.K882072ORTHOPAEDIC AND SPINAL RING CURRETTESKarlin Technology, 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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