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FDA 510(k)

X-TIP INTRAOSSEOUS PERFORATOR

K-Number: K990511 · 1999-04-27

ApplicantSchiff & Co.
Decision Date1999-04-27
Product CodeDZM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

X-TIP INTRAOSSEOUS PERFORATOR is the device name listed in this FDA 510(k) record. The listed applicant is Schiff & Co.. It received FDA 510(k) clearance on 1999-04-27 under 510(k) number K990511. The device is classified under product code DZM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-TIP INTRAOSSEOUS PERFORATOR?

X-TIP INTRAOSSEOUS PERFORATOR is a medical device that received FDA 510(k) clearance on 1999-04-27. The listed applicant is Schiff & Co.. The 510(k) number is K990511.

When did X-TIP INTRAOSSEOUS PERFORATOR receive FDA 510(k) clearance?

X-TIP INTRAOSSEOUS PERFORATOR received FDA 510(k) clearance on 1999-04-27, under 510(k) number K990511.

Who is the listed applicant for X-TIP INTRAOSSEOUS PERFORATOR?

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

What is the FDA product code for X-TIP INTRAOSSEOUS PERFORATOR?

The FDA product code for X-TIP INTRAOSSEOUS PERFORATOR is DZM.

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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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