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FDA 510(k)

SYNTHS ONE-THIRD TUBULAR DCL PLATE

K-Number: K011335 · 2001-07-27

ApplicantSynthes (Usa)
Decision Date2001-07-27
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHS ONE-THIRD TUBULAR DCL PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2001-07-27 under 510(k) number K011335. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHS ONE-THIRD TUBULAR DCL PLATE?

SYNTHS ONE-THIRD TUBULAR DCL PLATE is a medical device that received FDA 510(k) clearance on 2001-07-27. The listed applicant is Synthes (Usa). The 510(k) number is K011335.

When did SYNTHS ONE-THIRD TUBULAR DCL PLATE receive FDA 510(k) clearance?

SYNTHS ONE-THIRD TUBULAR DCL PLATE received FDA 510(k) clearance on 2001-07-27, under 510(k) number K011335.

Who is the listed applicant for SYNTHS ONE-THIRD TUBULAR DCL PLATE?

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

What is the FDA product code for SYNTHS ONE-THIRD TUBULAR DCL PLATE?

The FDA product code for SYNTHS ONE-THIRD TUBULAR DCL PLATE is HRS.

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.

Other records listing Synthes (Usa) 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.

View all 409 devices →

Related Devices (Code: HRS)

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.

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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