The following data is part of a premarket notification filed by Parcus Medical, Llc with the FDA for Parcus Peek Cf Push-in Suture Anchor.
Device ID | K102162 |
510k Number | K102162 |
Device Name: | PARCUS PEEK CF PUSH-IN SUTURE ANCHOR |
Classification | Screw, Fixation, Bone |
Applicant | PARCUS MEDICAL, LLC 839 SOUTH NEENAH AVE. Sturgeon Bay, WI 54235 |
Contact | Barton Bracy |
Correspondent | Barton Bracy PARCUS MEDICAL, LLC 839 SOUTH NEENAH AVE. Sturgeon Bay, WI 54235 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-02 |
Decision Date | 2010-11-10 |
Summary: | summary |