The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Peri-loc Periarticular Locked Plating System.
| Device ID | K062216 | 
| 510k Number | K062216 | 
| Device Name: | PERI-LOC PERIARTICULAR LOCKED PLATING SYSTEM | 
| Classification | Plate, Fixation, Bone | 
| Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 | 
| Contact | David Henley | 
| Correspondent | David Henley SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 | 
| Product Code | HRS | 
| CFR Regulation Number | 888.3030 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2006-08-01 | 
| Decision Date | 2006-09-15 | 
| Summary: | summary |