APOLLO KNEE TIBIAL BASEPLATE/KNEE TIBIAL INSERT— 510(k) K934381
Substantially Equivalent for Some IndicationsIntermedics Orthopedics
FDA 510(k) clearance K934381 for APOLLO KNEE TIBIAL BASEPLATE/KNEE TIBIAL INSERT, Substantially Equivalent for Some Indications on 1995-02-08. Applicant: Intermedics Orthopedics. Device class: 2.
Clearance details
- Applicant
- Intermedics Orthopedics
- Product code
- Code JWH
- Device class
- Class 2
- Regulation
- 21 CFR 888.3560
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Austin, TX, US
Recent devices under product code JWH
view allMore clearances from Intermedics Orthopedics
view allAdverse events under product code JWH
product code JWH- Death
- 26
- Injury
- 51,564
- Malfunction
- 9,725
- Other
- 9
- Total
- 61,324
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K934381
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K934381.
Data sourced from openFDA. This site is unofficial and independent of the FDA.