The following data is part of a premarket notification filed by Acumed, Inc. with the FDA for Cannulated Cancellous Bone Screw.
Device ID | K942341 |
510k Number | K942341 |
Device Name: | CANNULATED CANCELLOUS BONE SCREW |
Classification | Screw, Fixation, Bone |
Applicant | ACUMED, INC. 10950 S.W. 5TH ST. SUITE 170 Beaverton, OR 97005 |
Contact | Shari L Jeffers |
Correspondent | Shari L Jeffers ACUMED, INC. 10950 S.W. 5TH ST. SUITE 170 Beaverton, OR 97005 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-05-16 |
Decision Date | 1994-12-05 |