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FDA 510(k)

TAVA K-WIRE

K-Number: K940109 · 1994-02-22

ApplicantTava Surgical Instruments
Decision Date1994-02-22
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TAVA K-WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Tava Surgical Instruments. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K940109. 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 TAVA K-WIRE?

TAVA K-WIRE is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Tava Surgical Instruments. The 510(k) number is K940109.

When did TAVA K-WIRE receive FDA 510(k) clearance?

TAVA K-WIRE received FDA 510(k) clearance on 1994-02-22, under 510(k) number K940109.

Who is the listed applicant for TAVA K-WIRE?

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

What is the FDA product code for TAVA K-WIRE?

The FDA product code for TAVA K-WIRE is HTY.

Other records listing Tava Surgical Instruments 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.

K935367TAVA WIRE-DRIVERK885273MICRO SURGICAL INSTRUMENT SYSTEMK884492MICRO SURGICAL INSTRUMENT SYSTEMK872475SURGICAL BURK863788SAWBLADEK854543PULSE LAVAGE

View all 7 devices →

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.

K262722Primal K-Wire (P99-193-1410)Paragon 28, Inc.K253325ZipToe™ Hammertoe Fusion SystemToetal SolutionsK252657Impact PEEK Union Nail SystemNvision Biomedical Technologies, Inc.K250315RONAVIS – FX (FX-001)AIRS, Inc.K251362PediFlex™ Flexible Nail SystemOrthoPediatrics Corp.K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies

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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