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FDA 510(k)

GRAFT MARKER RING

K-Number: K001915 · 2001-04-27

ApplicantT. Korossurgical Instruments Corp.
Decision Date2001-04-27
Product CodeMAB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GRAFT MARKER RING is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 2001-04-27 under 510(k) number K001915. The device is classified under product code MAB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAFT MARKER RING?

GRAFT MARKER RING is a medical device that received FDA 510(k) clearance on 2001-04-27. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K001915.

When did GRAFT MARKER RING receive FDA 510(k) clearance?

GRAFT MARKER RING received FDA 510(k) clearance on 2001-04-27, under 510(k) number K001915.

Who is the listed applicant for GRAFT MARKER RING?

The FDA 510(k) record lists T. Korossurgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRAFT MARKER RING?

The FDA product code for GRAFT MARKER RING is MAB.

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Other records listing T. Korossurgical Instruments Corp. 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.

K002755NON-ABSORBING STERNATOMY MONOFILAMENT SUTUREK954016VIDEOSCOPE W/IRRIGATION SHEATHK953998DISCETOME TISSUE ASPIRATORK954052ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTESK954014PERCUTANEOUS DISCECTOMY CANNULA SYSTEMK935529CERVICAL SELF-RETAINING RETRACTOR

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Related Devices (Code: MAB)

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.

K052642SUTURING WASHERFirst Call, Inc.K894268C.A.B. RINGMedi-Sharp, 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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