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FDA 510(k)

TECHMEDICA DRILL GUIDE

K-Number: K841297 · 1984-04-25

ApplicantTechmedica, Inc.
Decision Date1984-04-25
Product CodeFZX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECHMEDICA DRILL GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K841297. The device is classified under product code FZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHMEDICA DRILL GUIDE?

TECHMEDICA DRILL GUIDE is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Techmedica, Inc.. The 510(k) number is K841297.

When did TECHMEDICA DRILL GUIDE receive FDA 510(k) clearance?

TECHMEDICA DRILL GUIDE received FDA 510(k) clearance on 1984-04-25, under 510(k) number K841297.

Who is the listed applicant for TECHMEDICA DRILL GUIDE?

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

What is the FDA product code for TECHMEDICA DRILL GUIDE?

The FDA product code for TECHMEDICA DRILL GUIDE is FZX.

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Other records listing Techmedica, Inc. as applicant

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K933935CKS POROUS COATED FEMORAL COMPONENTK932017TECHMEDICA CONTINUUM HIP WITH HA COATINGK931929TECHMEDICA CONTINUUM HIP SYSTEMK926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMK925420TECHMEDICA STANDARD BIPOLAR SYSTEMK923808MULLER STRAIGHT STEM FEMORAL PROSTHESIS

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Related Devices (Code: FZX)

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.

K914715PARALLELING GUIDESImplant Corp. of AmericaK871413CIVCO STEPPERCIVCO Medical Instruments Co., Inc.K871503BIOPSY NEEDLE GUIDE KIT, STERILEAmedic USAK862564A.C.L. GUIDE KITAspen Laboratories, Inc.K854262MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLYMeadox Surgimed, Inc.K852402NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZERNorth American Instrument 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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