FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OsseoFit Stemless Shoulder System
K Number: K241873
·
Decision Dec 11, 2024
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
18
Applicant Total
376
Review Days
167
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Basic Information
- Device Name
- OsseoFit Stemless Shoulder System
- K Number
- K241873
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3660
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Zimmer, Inc.
- Date Received
- June 27, 2024
- Decision Date
- December 11, 2024
- Product Code
- PKC
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PKC | Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained | FDA class 2 | Orthopedic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (PKC), ordered by most recent decision date.
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