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FDA 510(k)

SYNERGY TI ANTERIOR SPINAL SYSTEM

K-Number: K950709 · 1995-10-25

ApplicantCross Medical Products, Inc.
Decision Date1995-10-25
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

SYNERGY TI ANTERIOR SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cross Medical Products, Inc.. It received FDA 510(k) clearance on 1995-10-25 under 510(k) number K950709. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SYNERGY TI ANTERIOR SPINAL SYSTEM?

SYNERGY TI ANTERIOR SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1995-10-25. The listed applicant is Cross Medical Products, Inc.. The 510(k) number is K950709.

When did SYNERGY TI ANTERIOR SPINAL SYSTEM receive FDA 510(k) clearance?

SYNERGY TI ANTERIOR SPINAL SYSTEM received FDA 510(k) clearance on 1995-10-25, under 510(k) number K950709.

Who is the listed applicant for SYNERGY TI ANTERIOR SPINAL SYSTEM?

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

What is the FDA product code for SYNERGY TI ANTERIOR SPINAL SYSTEM?

The FDA product code for SYNERGY TI ANTERIOR SPINAL SYSTEM is KWQ.

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Other records listing Cross Medical Products, Inc. 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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Related Devices (Code: KWQ)

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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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