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FDA 510(k)

TAVA WIRE-DRIVER

K-Number: K935367 · 1994-04-21

ApplicantTava Surgical Instruments
Decision Date1994-04-21
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TAVA WIRE-DRIVER 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 1994-04-21 under 510(k) number K935367. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAVA WIRE-DRIVER?

TAVA WIRE-DRIVER is a medical device that received FDA 510(k) clearance on 1994-04-21. The listed applicant is Tava Surgical Instruments. The 510(k) number is K935367.

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

TAVA WIRE-DRIVER received FDA 510(k) clearance on 1994-04-21, under 510(k) number K935367.

Who is the listed applicant for TAVA WIRE-DRIVER?

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 WIRE-DRIVER?

The FDA product code for TAVA WIRE-DRIVER is HSZ.

Related Clinical Trials

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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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.

K940109TAVA K-WIREK885273MICRO SURGICAL INSTRUMENT SYSTEMK884492MICRO SURGICAL INSTRUMENT SYSTEMK872475SURGICAL BURK863788SAWBLADEK854543PULSE LAVAGE

View all 7 devices →

Related Devices (Code: HSZ)

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.

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical SystemsK972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SAK944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, Inc.

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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