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FDA 510(k)

GRAFT HARVESTING SAWBLADES

K-Number: K971978 · 1997-06-18

Decision Date1997-06-18
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRAFT HARVESTING SAWBLADES is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1997-06-18 under 510(k) number K971978. 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 GRAFT HARVESTING SAWBLADES?

GRAFT HARVESTING SAWBLADES is a medical device that received FDA 510(k) clearance on 1997-06-18. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K971978.

When did GRAFT HARVESTING SAWBLADES receive FDA 510(k) clearance?

GRAFT HARVESTING SAWBLADES received FDA 510(k) clearance on 1997-06-18, under 510(k) number K971978.

Who is the listed applicant for GRAFT HARVESTING 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 GRAFT HARVESTING SAWBLADES?

The FDA product code for GRAFT HARVESTING SAWBLADES is GFA.

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.

Other records listing Wrightmedicaltechnologyinc 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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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