The following data is part of a premarket notification filed by Smith & Nephew Endoscopy, Inc. with the FDA for Acufex Tibial Anchor Screw & Spiked Washer.
Device ID | K961649 |
510k Number | K961649 |
Device Name: | ACUFEX TIBIAL ANCHOR SCREW & SPIKED WASHER |
Classification | Screw, Fixation, Bone |
Applicant | SMITH & NEPHEW ENDOSCOPY, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
Contact | Tedd Gosian |
Correspondent | Tedd Gosian SMITH & NEPHEW ENDOSCOPY, INC. 130 FORBES BLVD. Mansfield, MA 02048 |
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 | 1996-04-30 |
Decision Date | 1996-07-16 |
Summary: | summary |