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FDA 510(k)

TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER

K-Number: K013923 · 2002-02-25

ApplicantBiomet Orthopedics, Inc.
Decision Date2002-02-25
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2002-02-25 under 510(k) number K013923. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER?

TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER is a medical device that received FDA 510(k) clearance on 2002-02-25. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K013923.

When did TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER receive FDA 510(k) clearance?

TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER received FDA 510(k) clearance on 2002-02-25, under 510(k) number K013923.

Who is the listed applicant for TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER?

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

What is the FDA product code for TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER?

The FDA product code for TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER is HSB.

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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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