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FDA 510(k)

ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES

K-Number: K070555 · 2007-07-13

ApplicantOrthopro, LLC
Decision Date2007-07-13
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Orthopro, LLC. It received FDA 510(k) clearance on 2007-07-13 under 510(k) number K070555. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES?

ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES is a medical device that received FDA 510(k) clearance on 2007-07-13. The listed applicant is Orthopro, LLC. The 510(k) number is K070555.

When did ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES receive FDA 510(k) clearance?

ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES received FDA 510(k) clearance on 2007-07-13, under 510(k) number K070555.

Who is the listed applicant for ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES?

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

What is the FDA product code for ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES?

The FDA product code for ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRES is HTY.

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Other records listing Orthopro, LLC 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.

K122936ANKLE TRAUMA SYSTEMK113006I-FUSE HAMMER TOE SYSTEMSK093055CSTS SCREWK073228DC ULNAR SHORTENING SYSTEMK071243METAL HEMI IMPLANTK062908ORTHROPRO HEMI TOE

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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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