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FDA 510(k)

SYNVASIVE CERAMIC SUTTING BLOCK

K-Number: K930573 · 1994-04-07

ApplicantSynvasive Technology, Inc.
Decision Date1994-04-07
Product CodeLXI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SYNVASIVE CERAMIC SUTTING BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Synvasive Technology, Inc.. It received FDA 510(k) clearance on 1994-04-07 under 510(k) number K930573. The device is classified under product code LXI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNVASIVE CERAMIC SUTTING BLOCK?

SYNVASIVE CERAMIC SUTTING BLOCK is a medical device that received FDA 510(k) clearance on 1994-04-07. The listed applicant is Synvasive Technology, Inc.. The 510(k) number is K930573.

When did SYNVASIVE CERAMIC SUTTING BLOCK receive FDA 510(k) clearance?

SYNVASIVE CERAMIC SUTTING BLOCK received FDA 510(k) clearance on 1994-04-07, under 510(k) number K930573.

Who is the listed applicant for SYNVASIVE CERAMIC SUTTING BLOCK?

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

What is the FDA product code for SYNVASIVE CERAMIC SUTTING BLOCK?

The FDA product code for SYNVASIVE CERAMIC SUTTING BLOCK is LXI.

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Related Devices (Code: LXI)

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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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