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FDA 510(k)

MITEK SUPER QUICKANCHOR, MODIFICATION

K-Number: K930893 · 1993-12-08

ApplicantMitek Surgical Products, Inc.
Decision Date1993-12-08
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MITEK SUPER QUICKANCHOR, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Surgical Products, Inc.. It received FDA 510(k) clearance on 1993-12-08 under 510(k) number K930893. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MITEK SUPER QUICKANCHOR, MODIFICATION?

MITEK SUPER QUICKANCHOR, MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-12-08. The listed applicant is Mitek Surgical Products, Inc.. The 510(k) number is K930893.

When did MITEK SUPER QUICKANCHOR, MODIFICATION receive FDA 510(k) clearance?

MITEK SUPER QUICKANCHOR, MODIFICATION received FDA 510(k) clearance on 1993-12-08, under 510(k) number K930893.

Who is the listed applicant for MITEK SUPER QUICKANCHOR, MODIFICATION?

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

What is the FDA product code for MITEK SUPER QUICKANCHOR, MODIFICATION?

The FDA product code for MITEK SUPER QUICKANCHOR, MODIFICATION is JDR.

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Other records listing Mitek Surgical Products, 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.

K953560MITEK THREADED ANCHOR (FASTIN)K953877MITEK GII ANCHORK936311MITEK MINI ANCHORK941599MITEK ABSORBABLE ANCHORK944051ABSORBALBE ANCHORK950070MITEK TOGGLE ANCHOR(TM)

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Related Devices (Code: JDR)

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.

K262451Arthrex DynaNite StaplesArthrex, Inc.K261121Megalodon Dynamic Compression SystemParagon 28, Inc.K250712Linkt Compression Staple SystemTrax SurgicalK243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemMedline Industries, LPK243742Arthrex DynaNite Nitinol StaplesArthrex, Inc.K243658TMC Compression Implant SystemTreace Medical Concepts

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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