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FDA 510(k)

SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS

K-Number: K081205 · 2008-07-01

ApplicantSynthes (Usa)
Decision Date2008-07-01
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2008-07-01 under 510(k) number K081205. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS?

SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS is a medical device that received FDA 510(k) clearance on 2008-07-01. The listed applicant is Synthes (Usa). The 510(k) number is K081205.

When did SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS receive FDA 510(k) clearance?

SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS received FDA 510(k) clearance on 2008-07-01, under 510(k) number K081205.

Who is the listed applicant for SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS?

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 SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS?

The FDA product code for SYNTHES (USA) 5.0MM/7.3MM CRIMP POSITIONING PINS is JDQ.

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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.

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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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