510(k) K852993

BONE RONGEURS by The Huxley Instrument Corp.

K852993 is an FDA 510(k) premarket notification submitted by The Huxley Instrument Corp. for the device "BONE RONGEURS". The FDA issued a decision of Substantially Equivalent on August 7, 1985. The Huxley Instrument Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1985
Date Received
July 15, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No