The following data is part of a premarket notification filed by Adaptive Specialty, Llc with the FDA for Adaptive Wedge.
| Device ID | K110662 |
| 510k Number | K110662 |
| Device Name: | ADAPTIVE WEDGE |
| Classification | Plate, Fixation, Bone |
| Applicant | ADAPTIVE SPECIALTY, LLC 1001 OAKWOOD BLVD Round Rock, TX 78681 |
| Contact | J.d. Webb |
| Correspondent | J.d. Webb ADAPTIVE SPECIALTY, LLC 1001 OAKWOOD BLVD Round Rock, TX 78681 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-03-08 |
| Decision Date | 2012-03-12 |
| Summary: | summary |