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FDA 510(k)

TITANIUM RODS

K-Number: K874612 · 1988-06-23

ApplicantMedical Marketing, Inc.
Decision Date1988-06-23
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TITANIUM RODS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing, Inc.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K874612. 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 TITANIUM RODS?

TITANIUM RODS is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Medical Marketing, Inc.. The 510(k) number is K874612.

When did TITANIUM RODS receive FDA 510(k) clearance?

TITANIUM RODS received FDA 510(k) clearance on 1988-06-23, under 510(k) number K874612.

Who is the listed applicant for TITANIUM RODS?

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

What is the FDA product code for TITANIUM RODS?

The FDA product code for TITANIUM RODS is HET.

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.

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Other records listing Medical Marketing, Inc. 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.

K874614SUCTION AND LAVAGE PROBEK874611TITANIUM BACKSTOP WITH SUCTIONK874615LASER CANNISTER FILTER

Related Devices (Code: HET)

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Official Source

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