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FDA 510(k)

ACE SCREW REMOVAL TREPHINE

K-Number: K882008 · 1988-06-10

ApplicantBuckman Co., Inc.
Decision Date1988-06-10
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACE SCREW REMOVAL TREPHINE is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1988-06-10 under 510(k) number K882008. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE SCREW REMOVAL TREPHINE?

ACE SCREW REMOVAL TREPHINE is a medical device that received FDA 510(k) clearance on 1988-06-10. The listed applicant is Buckman Co., Inc.. The 510(k) number is K882008.

When did ACE SCREW REMOVAL TREPHINE receive FDA 510(k) clearance?

ACE SCREW REMOVAL TREPHINE received FDA 510(k) clearance on 1988-06-10, under 510(k) number K882008.

Who is the listed applicant for ACE SCREW REMOVAL TREPHINE?

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

What is the FDA product code for ACE SCREW REMOVAL TREPHINE?

The FDA product code for ACE SCREW REMOVAL TREPHINE is HWE.

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Related Devices (Code: HWE)

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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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