The following data is part of a premarket notification filed by Ethicon, Inc. with the FDA for Ethicon Drill Bit And Drill Guide.
Device ID | K944590 |
510k Number | K944590 |
Device Name: | ETHICON DRILL BIT AND DRILL GUIDE |
Classification | Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment |
Applicant | ETHICON, INC. P.O BOX 151, ROUTE 22 WEST Somerville, NJ 08876 |
Contact | John D Paulson |
Correspondent | John D Paulson ETHICON, INC. P.O BOX 151, ROUTE 22 WEST Somerville, NJ 08876 |
Product Code | HSZ |
CFR Regulation Number | 878.4820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-09-19 |
Decision Date | 1995-05-11 |