510(k) K924381

PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS by Cross Medical Products, Inc. — Product Code KWP

K924381 is an FDA 510(k) premarket notification submitted by Cross Medical Products, Inc. for the device "PWB LUMBAR LAMINAR HOOKS WITH SET SCREWS". The FDA issued a decision of SN on May 18, 1993. The device falls under product code KWP (Appliance, Fixation, Spinal Interlaminal), a Class II device regulated under 21 CFR 888.3050. Cross Medical Products, Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
May 18, 1993
Date Received
August 31, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Appliance, Fixation, Spinal Interlaminal
Device Class
Class II
Regulation Number
888.3050
Review Panel
OR
Submission Type