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FDA 510(k)

MICRINS NEEDLE HOLDER

K-Number: K872989 · 1987-08-21

ApplicantMicrins Surgical, Inc.
Decision Date1987-08-21
Product CodeHXK
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MICRINS NEEDLE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Micrins Surgical, Inc.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K872989. The device is classified under product code HXK. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRINS NEEDLE HOLDER?

MICRINS NEEDLE HOLDER is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Micrins Surgical, Inc.. The 510(k) number is K872989.

When did MICRINS NEEDLE HOLDER receive FDA 510(k) clearance?

MICRINS NEEDLE HOLDER received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872989.

Who is the listed applicant for MICRINS NEEDLE HOLDER?

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

What is the FDA product code for MICRINS NEEDLE HOLDER?

The FDA product code for MICRINS NEEDLE HOLDER is HXK.

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.

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Other records listing Micrins Surgical, 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.

K993970MICRINS MICROSURGICAL SUTUREK982278MICRINS MICRO ANASTOMOSIS CLAMPK933310MICRINS CONTRAST BACKGROUND MATERIALK872991MICRINS FORCEPS 2010K872990MICRINS SURGICAL SCISSOR

Related Devices (Code: HXK)

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.

K890167HOLDER, NEEDLEDhason Brothers, Inc.K860018FISCHER WIRE/PIN CLAMPBuckman Co., Inc.K801594ACE FISCHER EXTERNAL FIXATION DEVICEAce Orthopedic Manufacturing Co.K772388CONVERSE-GILLIES NEEDLE HOLDEREdward Weck, 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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