The following data is part of a premarket notification filed by Cp Medical with the FDA for Cp Medical Bone Wax.
Device ID | K024372 |
510k Number | K024372 |
Device Name: | CP MEDICAL BONE WAX |
Classification | Wax, Bone |
Applicant | CP MEDICAL 836 N.E. 24TH AVE. Portland, OR 97232 |
Contact | Sue Ridge |
Correspondent | Sue Ridge CP MEDICAL 836 N.E. 24TH AVE. Portland, OR 97232 |
Product Code | MTJ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-12-31 |
Decision Date | 2003-06-19 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
20884521196268 | K024372 | 000 |