510(k) K935516

SNAP DRILL by Surgiquip, Inc. — Product Code HWE

K935516 is an FDA 510(k) premarket notification submitted by Surgiquip, Inc. for the device "SNAP DRILL". The FDA issued a decision of Substantially Equivalent on January 27, 1994. The device falls under product code HWE (Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment), a Class I device regulated under 21 CFR 878.4820. Surgiquip, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 27, 1994
Date Received
November 18, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Device Class
Class I
Regulation Number
878.4820
Review Panel
OR
Submission Type