SAWBLADE
K-Number: K863788 · 1986-10-14
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Device Summary
Frequently Asked Questions
What is the SAWBLADE?
SAWBLADE is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Tava Surgical Instruments. The 510(k) number is K863788.
When did SAWBLADE receive FDA 510(k) clearance?
SAWBLADE received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863788.
Who is the listed applicant for SAWBLADE?
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 SAWBLADE?
The FDA product code for SAWBLADE 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 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.
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
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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