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FDA 510(k)

WRIGHT MEDICAL TECHNOLOGY SAWBLADES

K-Number: K955229 · 1996-01-18

ApplicantWrightmedicaltechnologyinc
Decision Date1996-01-18
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WRIGHT MEDICAL TECHNOLOGY SAWBLADES is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1996-01-18 under 510(k) number K955229. The device is classified under product code GFA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIGHT MEDICAL TECHNOLOGY SAWBLADES?

WRIGHT MEDICAL TECHNOLOGY SAWBLADES is a medical device that received FDA 510(k) clearance on 1996-01-18. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K955229.

When did WRIGHT MEDICAL TECHNOLOGY SAWBLADES receive FDA 510(k) clearance?

WRIGHT MEDICAL TECHNOLOGY SAWBLADES received FDA 510(k) clearance on 1996-01-18, under 510(k) number K955229.

Who is the listed applicant for WRIGHT MEDICAL TECHNOLOGY SAWBLADES?

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

What is the FDA product code for WRIGHT MEDICAL TECHNOLOGY SAWBLADES?

The FDA product code for WRIGHT MEDICAL TECHNOLOGY SAWBLADES is GFA.

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Related Devices (Code: GFA)

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.

K971978GRAFT HARVESTING SAWBLADESWrightmedicaltechnologyincK954483STRYKER SAGITTAL SAW ATTACHMENTStryker InstrumentsK953012DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLSBoston Surgical Products, Inc.K950403SURGICAL SAW BLADESTransidyne General Corp.K940501RE-SHARPENABLE SAW BLADESAdven MedicalK933595BUR, SURGICAL, GENERAL & PLASTIC SURGERYOmega Surgical Instruments, 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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