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FDA 510(k)

SYNTHES WIRE MOUNT

K-Number: K953777 · 1996-03-08

ApplicantSynthes (Usa)
Decision Date1996-03-08
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES WIRE MOUNT is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1996-03-08 under 510(k) number K953777. 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 WIRE MOUNT?

SYNTHES WIRE MOUNT is a medical device that received FDA 510(k) clearance on 1996-03-08. The listed applicant is Synthes (Usa). The 510(k) number is K953777.

When did SYNTHES WIRE MOUNT receive FDA 510(k) clearance?

SYNTHES WIRE MOUNT received FDA 510(k) clearance on 1996-03-08, under 510(k) number K953777.

Who is the listed applicant for SYNTHES WIRE MOUNT?

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 WIRE MOUNT?

The FDA product code for SYNTHES WIRE MOUNT 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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