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FDA 510(k)

RIDIDFIX 2.7MM BTB CROSS PIN KIT

K-Number: K013781 · 2002-02-06

ApplicantMitek Products
Decision Date2002-02-06
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RIDIDFIX 2.7MM BTB CROSS PIN KIT is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Products. It received FDA 510(k) clearance on 2002-02-06 under 510(k) number K013781. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIDIDFIX 2.7MM BTB CROSS PIN KIT?

RIDIDFIX 2.7MM BTB CROSS PIN KIT is a medical device that received FDA 510(k) clearance on 2002-02-06. The listed applicant is Mitek Products. The 510(k) number is K013781.

When did RIDIDFIX 2.7MM BTB CROSS PIN KIT receive FDA 510(k) clearance?

RIDIDFIX 2.7MM BTB CROSS PIN KIT received FDA 510(k) clearance on 2002-02-06, under 510(k) number K013781.

Who is the listed applicant for RIDIDFIX 2.7MM BTB CROSS PIN KIT?

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

What is the FDA product code for RIDIDFIX 2.7MM BTB CROSS PIN KIT?

The FDA product code for RIDIDFIX 2.7MM BTB CROSS PIN KIT is HTY.

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Other records listing Mitek Products 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.

K013572MITEK BIOCRYL INTERFERENCE SCREWSK002639BIOKNOTLESS ANCHORK010633RIGIDFIX SOFT TISSUE ACL CROSSPIN SYSTEMK002406MITEK 2GII MENISCAL REPAIR SYSTEMK003076MITEK CUFFTACKK002422VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM

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Related Devices (Code: HTY)

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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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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