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FDA 510(k)

CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.)

K-Number: K904446 · 1991-09-05

ApplicantAcromed Corp.
Decision Date1991-09-05
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) is the device name listed in this FDA 510(k) record. The listed applicant is Acromed Corp.. It received FDA 510(k) clearance on 1991-09-05 under 510(k) number K904446. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.)?

CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) is a medical device that received FDA 510(k) clearance on 1991-09-05. The listed applicant is Acromed Corp.. The 510(k) number is K904446.

When did CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) receive FDA 510(k) clearance?

CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) received FDA 510(k) clearance on 1991-09-05, under 510(k) number K904446.

Who is the listed applicant for CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.)?

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

What is the FDA product code for CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.)?

The FDA product code for CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) is 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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