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FDA 510(k)

MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY

K-Number: K990372 · 1999-10-14

ApplicantDr. Fritz GmbH
Decision Date1999-10-14
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Fritz GmbH. It received FDA 510(k) clearance on 1999-10-14 under 510(k) number K990372. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY?

MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Dr. Fritz GmbH. The 510(k) number is K990372.

When did MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY receive FDA 510(k) clearance?

MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY received FDA 510(k) clearance on 1999-10-14, under 510(k) number K990372.

Who is the listed applicant for MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY?

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

What is the FDA product code for MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY?

The FDA product code for MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY is HET.

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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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