The following data is part of a premarket notification filed by Link America, Inc. with the FDA for Link Dynamic Staple.
| Device ID | K853704 |
| 510k Number | K853704 |
| Device Name: | LINK DYNAMIC STAPLE |
| Classification | Staple, Fixation, Bone |
| Applicant | LINK AMERICA, INC. C/O SURGICAL IMPLANTS, INC. 10 GREAT MEADOW LANE East Hanavor, NJ 07936 |
| Contact | Edward Schussler |
| Correspondent | Edward Schussler LINK AMERICA, INC. C/O SURGICAL IMPLANTS, INC. 10 GREAT MEADOW LANE East Hanavor, NJ 07936 |
| Product Code | JDR |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-09-04 |
| Decision Date | 1986-01-21 |