510(k) K951492

RIB RESECTOR by United States Surgical, A Division of Tyco Healthc — Product Code HAO

K951492 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "RIB RESECTOR". The FDA issued a decision of Substantially Equivalent on May 18, 1995. The device falls under product code HAO (Instrument, Surgical, Non-Powered), a Class I device regulated under 21 CFR 882.4535. United States Surgical, A Division of Tyco Healthc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 18, 1995
Date Received
March 31, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Surgical, Non-Powered
Device Class
Class I
Regulation Number
882.4535
Review Panel
NE
Submission Type