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FDA 510(k)

MODIFIED PODIATRY PRODUCTS

K-Number: K771006 · 1977-06-17

ApplicantDentronix, Inc.
Decision Date1977-06-17
Product CodeHTZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED PODIATRY PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Dentronix, Inc.. It received FDA 510(k) clearance on 1977-06-17 under 510(k) number K771006. The device is classified under product code HTZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED PODIATRY PRODUCTS?

MODIFIED PODIATRY PRODUCTS is a medical device that received FDA 510(k) clearance on 1977-06-17. The listed applicant is Dentronix, Inc.. The 510(k) number is K771006.

When did MODIFIED PODIATRY PRODUCTS receive FDA 510(k) clearance?

MODIFIED PODIATRY PRODUCTS received FDA 510(k) clearance on 1977-06-17, under 510(k) number K771006.

Who is the listed applicant for MODIFIED PODIATRY PRODUCTS?

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

What is the FDA product code for MODIFIED PODIATRY PRODUCTS?

The FDA product code for MODIFIED PODIATRY PRODUCTS is HTZ.

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Other records listing Dentronix, 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.

K910202DENTRONIX MODEL 2000K880322DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEMK771005NEW PODIATRY PRODUCTSK770305CUTTER, P607 BONEK770302CUTTER, P606 BONEK770303NIPPER, NAIL, P610 ENGLISH

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Related Devices (Code: HTZ)

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.

K933933CEBOPLANESynvasive Technology, Inc.K931737HEDLEYL INTRAMEDULLARY PREPARATION BRUSHSynvasive Technology, Inc.K87088245 DEGREE SHAVERBowen & Company, Inc.K853678KAMBIN SPINAL INSTRUMENT SETPilling Co.K850423CONCEPT SUCTION SLEEVEConcept, Inc.K850527ARTHROSCOPY SUCTION BIOPSY PUNCHT. Korossurgical Instruments Corp.

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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