510(k) K822554

CEMENT EXTRACTION INSTRUMENTATION by Surgi-Quip Inc.U

K822554 is an FDA 510(k) premarket notification submitted by Surgi-Quip Inc.U for the device "CEMENT EXTRACTION INSTRUMENTATION". The FDA issued a decision of Substantially Equivalent on September 14, 1982. Surgi-Quip Inc.U has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1982
Date Received
August 24, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No