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FDA 510(k)

ACE MOS SAW AND THE ACE MOS SPINE SAW

K-Number: K862504 · 1986-08-07

ApplicantBuckman Co., Inc.
Decision Date1986-08-07
Product CodeJDX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE MOS SAW AND THE ACE MOS SPINE SAW 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 1986-08-07 under 510(k) number K862504. The device is classified under product code JDX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE MOS SAW AND THE ACE MOS SPINE SAW?

ACE MOS SAW AND THE ACE MOS SPINE SAW is a medical device that received FDA 510(k) clearance on 1986-08-07. The listed applicant is Buckman Co., Inc.. The 510(k) number is K862504.

When did ACE MOS SAW AND THE ACE MOS SPINE SAW receive FDA 510(k) clearance?

ACE MOS SAW AND THE ACE MOS SPINE SAW received FDA 510(k) clearance on 1986-08-07, under 510(k) number K862504.

Who is the listed applicant for ACE MOS SAW AND THE ACE MOS SPINE SAW?

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 MOS SAW AND THE ACE MOS SPINE SAW?

The FDA product code for ACE MOS SAW AND THE ACE MOS SPINE SAW is JDX.

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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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